|Publication number||US6682734 B1|
|Application number||US 08/475,813|
|Publication date||Jan 27, 2004|
|Filing date||Jun 7, 1995|
|Priority date||Nov 13, 1992|
|Also published as||CA2149329A1, CA2149329C, DE69303494D1, DE69303494T2, DE69329503D1, DE69329503T2, DE122004000036I1, EP0669836A1, EP0669836B1, EP0752248A1, EP0752248B1, EP1005870A2, EP1005870A3, EP1005870B1, US5776456, US5843439, US6399061, US7381560, US7422739, US20020197255, US20030021781, US20030095963, US20050186205, US20080089893, WO1994011026A2, WO1994011026A3|
|Publication number||08475813, 475813, US 6682734 B1, US 6682734B1, US-B1-6682734, US6682734 B1, US6682734B1|
|Inventors||Darrell R. Anderson, Nabil Hanna, John E. Leonard, Roland A. Newman, Mitchell E. Reff, William H. Rastetter|
|Original Assignee||Idec Pharmaceuticals Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (8), Non-Patent Citations (5), Referenced by (104), Classifications (63), Legal Events (6)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a divisional of application Ser. No. 08/149,099, filed Nov. 3, 1993, now U.S. Pat. No. 5,736,137, which is a Continuation-in-Part of U.S. Ser. No. 07/978,891, filed Nov. 13. 1992, now abandoned. This patent document is related to U.S. Ser. No. 07/9177,691 now abandoned entitled, “IMPAIRED DOMINANT SELECTABLE MARKER SEQUENCE FOR ENHANCEMENT OF EXPRESSION OF CO-LINKED GENE PRODUCT AND EXPRESSION VECTOR SYSTEMS COMPRISING SAME” (filed Nov. 13, 1992, now abandoned) and “IMPAIRED DOMINANT SELECTABLE MARKER SEQUENCE AND INTRONIC INSERTION STRATEGIES FOR ENHANCEMENT OF EXPRESSION OF GENE PRODUCT AND EXPRESSION VECTOR SYSTEMS COMPRISING SAME,” U.S. Ser. No. 08/147,696, now U.S. Pat. No. 5,648,267. The related patent documents are incorporated herein by reference.
A portion of the disclosure of this patent document contains material which is subject to copyright protection. The copyright owner does not object to the reproduction by anyone of the patent document or the patent disclosure, as it appears in the Patent and Trademark Office patent files or records, but otherwise reserves all copyright rights whatsoever.
The references to be discussed throughout this document are set forth merely for the information described therein prior to the filing dates of this document, and nothing herein is to be construed as an admission, either express or implied, that the references are “prior art” or that the inventors are not entitled to antedate such descriptions by virtue of prior inventions or priority based on earlier filed applications.
The present invention is directed to the treatment of B cell lymphoma using chimeric and radiolabeled antibodies to the B cell surface antigen Bp35 (“CD20”).
The immune system of vertebrates (for example, primates, which include humans, apes, monkeys, etc.) consists of a number of organs and cell types which have evolved to: accurately and specifically recognize foreign microorganisms (“antigen”) which invade the vertebrate-host; specifically bind to such foreign microorganisms; and, eliminate/destroy such foreign microorganisms. Lymphocytes, amongst others, are critical to the immune system. Lymphocytes are produced in the thymus, spleen and bone marrow (adult) and represent about 30% of the total white blood cells present in the circulatory system of humans (adult). There are two major sub-populations of lymphocytes: T cells and B cells. T cells are responsible for cell mediated immunity, while B cells are responsible for antibody production (humoral immunity). However, T cells and B cells can be considered as interdependent—in a typical immune response, T cells are activated when the T cell receptor binds to fragments of an antigen that are bound to major histocompatability complex (“MHC”) glycoproteins on the surface of an antigen presenting cell; such activation causes release of biological mediators (“interleukins”) which, in essence, stimulate B cells to differentiate and produce antibody (“immunoglobulins”) against the antigen.
Each B call within the host expresses a different antibody on its surface—thus, one B cell will express antibody specific for one antigen, while another B cell will express antibody specific for a different antigen. Accordingly, B cells are quite diverse, and this diversity is critical to the immune system. In humans, each B cell can produce an enormous number of antibody molecules (ie, about 107 to 108). Such antibody production most typically ceases (or substantially decreases) when the foreign antigen has been neutralized. Occasionally, however, proliferation of a particular B cell will continue unabated; such proliferation can result in a cancer referred to as “B cell lymphoma.”
T cells and B cells both comprise cell surface proteins which can be utilized as “markers” for differentiation and identification. One such human B cell marker is the human B lymphocyte-restricted differentiation antigen Bp35, referred to as “CD20. ” CD20 is expressed during early pre-B cell development and remains until plasma cell differentiation. Specifically, the CD20 molecule may regulate a step in the activation process which is required for cell cycle initiation and differentiation and is usually expressed at very high levels on neoplastic (“tumor”) B cells. CD20, by definition, is present on both “normal” B cells as well as “malignant” B cells, ie, those B cells whose unabated proliferation can lead to B cell lymphoma. Thus, the CD20 surface antigen has the potential of serving as a candidate for “targeting” of B cell lymphomas.
In essence, such targeting can be generalized as follows: antibodies specific to the CD20 surface antigen of B cells are, eg, injected into a patient. These anti-CD20 antibodies specifically bind to the CD20 cell surface antigen of (ostensibly) both normal and malignant B cells; the anti-CD20 antibody bound to the CD20 surface antigen may lead to the destruction and depletion of neoplastic B cells. Additionally, chemical agents or radioactive labels having the potential to destroy the tumor can be conjugated to the anti-CD20 antibody such that the agent is specifically “delivered” to, eg, the neoplastic B cells. Irrespective of the approach, a primary goal is to destroy the tumor: the specific approach can be determined by the particular anti-CD20 antibody which is utilized and, thus, the available approaches to targeting the CD20 antigen can vary considerably.
For example, attempts at such targeting of CD20 surface antigen have been reported. Murine (mouse) monoclonal antibody 1F5 (an anti-CD20 antibody) was reportedly administered by continuous intravenous infusion to B cell lymphoma patients. Extremely high levels (>2 grams) of 1F5 were reportedly required to deplete circulating tumor cells, and the results were described as being “transient.” Press et al., “Monoclonal Antibody 1F5 (Anti-CD20) Serotherapy of Human B-Cell Lymphomas.” Blood 69/2:584-591 (1987). A potential problem with this approach is that non-human monoclonal antibodies (eg, murine monoclonal antibodies) typically lack human effector functionality, ie, they are unable to, inter alia, mediate complement dependent lysis or lyse human target cells through antibody dependent cellular toxicity or Fc-receptor mediated phagocytosis. Furthermore, non-human monoclonal antibodies can be recognized by the human host as a foreign protein; therefore, repeated injections of such foreign antibodies can lead to the induction of immune responses leading to harmful hypersensitivity reactions. For murine-based monoclonal antibodies, this is often referred to as a Human Anti-Mouse Antibody response, or “HAMA” response. Additionally, these “foreign” antibodies can be attacked by the immune system of the host such that they are, in effect, neutralized before they reach their target site.
Lymphocytes and lymphoma cells are inherently sensitive to radiotherapy for several reasons: the local emission of ionizing radiation of radiolabeled antibodies may kill cells with or without the target antigen (eg, CD20) in close proximity to antibody bound to the antigen; penetrating radiation may obviate the problem of limited access to the antibody in bulky or poorly vascularized tumors; and, the total amount of antibody required may be reduced. The radionuclide emits radioactive particles which can damage cellular DNA to the point where the cellular repair mechanisms are unable to allow the cell to continue living; therefore, if the target cells are tumors, the radioactive label beneficially kills the tumor cells. Radiolabeled antibodies, by definition, include the use of a radioactive substance which may require the need for precautions for both the patient (ie, possible bone marrow transplantation) as well as the health care provider (ie, the need to exercise a high degree of caution when working with the radioactivity).
Therefore, an approach at improving the ability of murine monoclonal antibodies to be effective in the treatment of B-cell disorders has been to conjugate a radioactive label or toxin to the antibody such that the label or toxin is localized at the tumor site. For example, the above-referenced IF5 antibody has been “labeled” with iodine-131 (“131I”) and was reportedly evaluated for biodistribution in two patients. See Eary, J. F. et al., “Imaging and Treatment of B-Cell Lymphoma” J. Nuc. Med. 31/8:1257-1268 (1990); see also, Press, O. W. et al., “Treatment of Refractory Non-Hodgkin's Lymphoma with Radiolabeled MB-1 (Anti-CD37) Antibody” J. Clin. Onc. 7/8:1027-1038 (1989) (indication that one patient treated with 131I-labeled IF-5 achieved a “partial response”); Goldenberg, D. M. et al., “Targeting, Dosimetry and Radioimmunotherapy of B-Cell Lymphomas with Iodine-131-Labeled LL2 Monoclonal Antibody” J. Clin. Onc. 9/4:548-564 (1991) (three of eight patients receiving multiple injections reported to have developed a HAMA response); Appelbaum, F. R. “Radiolabeled Monoclonal Antibodies in the Treatment of Non-Hodgkin's Lymphoma” Hem./Onc. Clinics of N.A. 5/5:1013-1025 (1991) (review article); Press, O. W. et al “Radiolabeled-Antibody Therapy of B-Cell Lymphoma with Autologous Bone Marrow Support.” New England Journal of Medicine 329/17: 1219-12223 (1993) (iodine-131 labeled anti-CD20 antibody IF5 and B1); and Kaminski, M. G. et al “Radioimmunotherapy of B-Cell Lymphoma with [131I] Anti-B1 (Anti-CD20) Antibody”. NEJM 329/7 (1993) (iodine-131 labeled anti-CD20 antibody B1; hereinafter “Kaminski”).
Toxins (ie, chemotherapeutic agents such as doxorubicin or mitomycin C) have also been conjugated to antibodies. See, for example, PCT published application WO 92/07466 (published May 14, 1992).
“Chimeric” antibodies, ie, antibodies which comprise portions from two or more different species (eg, mouse and human) have been developed as an alternative to “conjugated” antibodies. For example, Liu, A. Y. et al., “Production of a Mouse-Human Chimeric Monoclonal Antibody to CD20 with Potent Fc-Dependent Biologic Activity” J. Immun. 139/10:3521-3526 (1987), describes a mouse/human chimeric antibody directed against the CD20 antigen. See also, PCT Publication No. WO 88/04936. However, no information is provided as to the ability, efficacy or practicality of using such chimeric antibodies for the treatment of B cell disorders in the reference. It is noted that in vitro functional assays (eg, complement dependent lysis (“CDC”); antibody dependent cellular cytotoxicity (“ADCC”), etc.) cannot inherently predict the in vivo capability of a chimeric antibody to destroy or deplete target cells expressing the specific antigen. See, for example, Robinson, R. D. et al., “Chimeric mouse-human anti-carcinoma antibodies that mediate different anti-tumor cell biological activities,” Hum. Antibod. Hybridomas 2:84-93 (1991) (chimeric mouse-human antibody having undetectable ADCC activity). Therefore, the potential therapeutic efficacy of chimeric antibody can only truly be assessed by in vivo experimentation.
What is needed, and what would be a great advance in the art, are therapeutic approaches targeting the CD20 antigen for the treatment of B cell lymphomas in primates, including, but not limited to, humans.
Disclosed herein are therapeutic methods designed for the treatment of B cell disorders, and in particular, B cell lymphomas. These protocols are based upon the administration of immunologically active chimeric anti-CD20 antibodies for the depletion of peripheral blood B cells, including B cells associated with lymphoma; administration of radiolabeled anti-CD20 antibodies for targeting localized and peripheral B cell associated tumors; and administration of chimeric anti-CD20 antibodies and radiolabeled anti-CD20 antibodies in a cooperative therapeutic strategy.
FIG. 1 is a diagrammatic representation of a tandem chimeric antibody expression vector useful in the production of immunologically active chimeric anti-CD20 antibodies (“TCAE 8”);
FIGS. 2A through 2H are nucleic acid sequences contained in the vector of FIG. 1;
FIGS. 3A through 3H contains the nucleic acid sequence of the vector of FIG. 1 further comprising murine light and heavy chain variable regions (“anti-CD20 in TCAE 8”);
FIG. 4 is the nucleic acid and amino acid sequences (including CDR and framework regions) of murine variable region light chain derived from murine anti-CD20 monoclonal antibody 2B8 (SEQ ID. NO:3-4);
FIG. 5 is the nucleic acid and amino acid sequences (including CDR and framework regions) of murine variable region heavy chain derived from murine anti-CD20 monoclonal antibody 2B8 (SEQ ID. NO:5-6);
FIG. 6 are flow cytometry results evidencing binding of fluorescent-labeled human C1q to chimeric anti-CD20 antibody, including, as controls labeled C1q; labeled C1q and murine anti-CD20 monoclonal antibody 2B8; and labeled C1q and human IgGl,k;
FIG. 7 represents the results of complement related lysis comparing chimeric anti-CD20 antibody and murine anti-CD20 monoclonal antibody 2B8;
FIG. 8 represents the results of antibody mediated cellular cytotoxicity with in vivo human effector cells comparing chimeric anti-CD20 antibody and 2B8;
FIGS. 9A, 9B and 9C provide the results of non-human primate peripheral blood B lymphocyte depletion after infusion of 0.4 mg/kg (A); 1.6 mg/kg (B); and 6.4 mg/kg (C) of immunologically active chimeric anti-CD20 antibody;
FIG. 10 provides the results of, inter alia, non-human primate peripheral blood B lymphocyte depletion after infusion of 0.01 mg/kg of immunologically active chimeric anti-CD20 antibody;
FIG. 11 provides results of the tumoricidal impact of Y2B8 in a mouse xenographic model utilizing a B cell lymphoblastic tumor;
FIG. 12 provides results of the tumoricidal impact of C2B8 in a mouse xenographic model utilizing a B cell lymphoblastic tumor;
FIG. 13 provides results of the tumoricidal impact of a combination of Y2B8 and C2B8 in a mouse xenographic model utilizing a B cell lymphoblastic tumor; and
FIGS. 14A and 14B provide results from a Phase I/II clinical analysis of C2B8 evidencing B-cell population depletion over time for patients evidencing a partial remission of the disease (14A) and a minor remission of the disease (14B).
Generally, antibodies are composed of two light chains and two heavy chain molecules; these chains form a general “Y” shape, with both light and heavy chains forming the arms of the Y and the heavy chains forming the base of the Y. Light and heavy chains are divided into domains of structural and functional homology. The variable domains of both the light (“VL”) and the heavy (“VH”) chains determine recognition and specificity. The constant region domains of light (“CL”) and heavy (“CH”) chains confer important biological properties, eg antibody chain association, secretion, transplacental mobility, Fc receptor binding complement binding, etc. The series of events leading to immunoglobulin gene expression in the antibody producing cells are complex. The variable domain region gene sequences are located in separate germ line gene segments referred to as “VH,” “D,” and “JH,” or “VL” and “JL.” These gene segments are joined by DNA rearrangements to form the complete V regions expressed in heavy and light chains, respectively. The rearranged, joined V segments (VL-JLand VH-D-JH) then encode the complete variable regions or antigen binding domains of light and heavy chains, respectively.
Serotherapy of human B call lymphomas using an anti-CD20 murine monoclonal antibody (1F5) has been described by Press et al., (69 Blood 584, 1987, supra); the reported therapeutic responses, unfortunately, were transient. Additionally, 25% of the tested patients reportedly developed a human anti-mouse antibody (HAMA) response to the serotherapy. Press et al., suggest that these antibodies, conjugated to toxins or radioisotopes, might afford a more lasting clinical benefit than the unconjugated antibody.
Owing to the debilitating effects of B cell lymphoma and the very real need to provide viable treatment approaches to this disease, we have embarked upon different approaches having a particular antibody, 2B8, as the common link between the approaches. One such approach advantageously exploits the ability of mammalian systems to readily and efficiently recover peripheral blood B cells; using this approach, we seek to, in essence, purge or deplete B cells in peripheral blood and lymphatic tissue as a means of also removing B cell lymphomas. We accomplish this by utilization of, inter alia, immunologically active, chimeric anti-CD20 antibodies. In another approach, we seek to target tumor cells for destruction with radioactive labels.
As used herein, the term “anti-CD20 antibody” is an antibody which specifically recognizes a cell surface non-glycosylated phosphoprotein of 35,000 Daltons, typically designated as the human B lymphocyte restricted differentiation antigen Bp35, commonly referred to as CD20. As used herein, the term “chimeric” when used in reference to anti-CD20 antibodies, encompasses antibodies which are most preferably derived using recombinant deoxyribonucleic acid techniques and which comprise both human (including immunologically “related” species, eg, chimpanzee) and non-human components: the constant region of the chimeric antibody is most preferably substantially identical to the constant region of a natural human antibody; the variable region of the chimeric antibody is most preferably derived from a non-human source and has the desired antigenic and specificity to the CD20 cell surface antigen. The non-human source can be any vertebrate source which can be used to generate antibodies to a human CD20 cell surface antigen or material comprising a human CD20 cell surface antigen. Such non-human source includes, but is not limited to, rodents (eg, rabbit, rat, mouse, etc.) and non-human primates (eg, Old World Monkey, Ape, etc.). Most preferably, the non-human component (variable region) is derived from a murine source. As used herein, the phrase “immunologically active” when used in reference to chimeric anti-CD20 antibodies, means a chimeric antibody which binds human C1q, mediates complement dependent lysis (“CDC”) of human B lymphoid cell lines, and lyses human target cells through antibody dependent cellular cytotoxicity (“ADCC”). As used herein, the phrases “indirect labeling” and “indirect labeling approach” both mean that a chelating agent is covalently attached to an antibody and at least one radionuclide is inserted into the chelating agent. Preferred chelating agents and radionuclides are set forth in Srivagtava, S. C. and Mease, R. C., “Progress in Research on Ligands, Nuclides and Techniques for Labeling Monoclonal Antibodies,” Nucl. Med. Bio. 18/6: 589-603 (1991) (“Srivagtava”) which is incorporated herein by reference. A particularly preferred chelating agent is 1-isothiocycmatobenzyl-3-methyldiothelene triaminepent acetic acid (“MX-DTPA”); particularly preferred radionuclides for indirect labeling include indium  and yttrium . As used herein, the phrases “direct labeling” and “direct labeling approach” both mean that a radionuclide is covalently attached directly to an antibody (typically via an amino acid residue). Preferred radionuclides are provided in Srivagtava; a particularly preferred radionuclide for direct labeling is iodine  covalently attached via tyrosine residues. The indirect labeling approach is particularly preferred.
The therapeutic approaches disclosed heroin are based upon the ability of the immune system of primates to rapidly recover, or rejuvenate, peripheral blood B cells. Additionally, because the principal immune response of primates is occasioned by T cells, when the immune system has a peripheral blood B cell deficiency, the need for “extraordinary” precautions (ie, patient isolation, etc.) is not necessary. As a result of these and other nuances of the immune systems of primates, our therapeutic approach to B cell disorders allows for the purging of peripheral blood B cells using immunologically active chimeric anti-CD20 antibodies.
Because peripheral blood B cell disorders, by definition, can indicate a necessity for access to the blood for treatment, the route of administration of the immunologically active chimeric anti-CD20 antibodies and radioalabeled anti-CD20 antibodies is preferably parenteral; as used herein, the term “parenteral” includes intravenous, intramuscular, subcutaneous, rectal, vaginal or intraperitoneal administration. Of these, intravenous administration is most preferred.
The immunologically active chimeric anti-CD20 antibodies and radiolabeled anti-CD20 antibodies will typically be provided by standard technique within a pharmaceutically acceptable buffer, for example, sterile saline, sterile buffered water, propylene glycol, combinations of the foregoing, etc. Methods for preparing parenternally administerable agents are described in Pharmaceutical Carriers & Formulations, Martin, Remington's Pharmaceutical Sciences, 15th Ed. (Mack Pub. Co., Easton, Pa. 1975), which is incorporated herein by reference.
The specific, therapeutically effective amount of immunologically active chimeric anti-CD20 antibodies useful to produce a unique therapeutic effect in any given patient can be determined by standard techniques well known to those of ordinary skill in the art.
Effective dosages (ie, therapeutically effective amounts) of the immunologically active chimeric anti-CD20 antibodies range from about 0.001 to about 30 mg/kg body weight, more preferably from about 0.01 to about 25 mg/kg body weight, and most preferably from about 0.4 to about 20.0 mg/kg body weight. Other dosages are viable; factors influencing dosage include, but are not limited to, the severity of the disease; previous treatment approaches; overall health of the patient; other diseases present, etc. The skilled artisan is readily credited with assessing a particular patient and determining a suitable dosage that falls within the ranges, or if necessary, outside of the ranges.
Introduction of the immunologically active chimeric anti-CD20 antibodies in these dose ranges can be carried out as a single treatment or over a series of treatments. With respect to chimeric antibodies, it is preferred that such introduction be carried out over a series of treatments; this preferred approach is predicated upon the treatment methodology associated with this disease. While not wishing to be bound by any particular theory, because the immunologically active chimeric anti-CD20 antibodies are both immunologically active and bind to CD20, upon initial introduction of the immunologically active chimeric anti-CD20 antibodies to the individual, peripheral blood B cell depletion will begin; we have observed a nearly complete depletion within about 24 hours post treatment infusion. Because of this, subsequent introduction(s) of the immunologically active chimeric anti-CD20 antibodies (or radiolabeled anti-CD20 antibodies) to the patient is presumed to: a) clear remaining peripheral blood B cells; b) begin B cell depletion from lymph nodes; c) begin B cell depletion from other tissue sources, eg, bone marrow, tumor, etc. Stated again, by using repeated introductions of the immunologically active chimeric anti-CD20 antibodies, a series of events take place, each event being viewed by us as important to effective treatment of the disease, The first “event” then, can be viewed as principally directed to substantially depleting the patient's peripheral blood B cells; the subsequent “events” can be viewed as either principally directed to simultaneously or serially clearing remaining B cells from the system clearing lymph node B cells, or clearing other tissue B cells.
In effect, while a single dosage provides benefits and can be effectively utilized for disease treatment/management, a preferred treatment course can occur over several stages; most preferably, between about 0.4 and about 20 mg/kg body weight of the immunologically active chimeric anti-CD20 antibodies is introduced to the patient once a week for between about 2 to 10 weeks, most preferably for about 4 weeks.
With reference to the use of radiolabeled anti-CD20 antibodies, a preference is that the antibody is non-chimeric; this preference is predicted upon the significantly longer circulating half-life of chimeric antibodies vis-a-vis murine antibodies (ie, with a longer circulating half-life, the radionuclide is present in the patient for extended periods). However, radiolabeled chimeric antibodies can be beneficially utilized with lower milli-Curries (“mCi”) dosages used in conjunction with the chimeric antibody relative to the murine antibody. This scenario allows for a decrease in bone marrow toxicity to an acceptable level, while maintaining therapeutic utility.
A variety of radionuclides are applicable to the present invention and those skilled in the art are credited with the ability to readily determine which radionuclide is most appropriate under a variety of circumstances. For example, iodine  is a well known radionuclide used for targeted immunotherapy. However, the clinical usefulness of iodine  can be limited by several factors including: eight-day physical half-life; dehalogenation of iodinated antibody both in the blood and at tumor sites; and emission characteristics (eg, large gamma component) which can be suboptimal for localized dose deposition in tumor. With the advent of superior chelating agents, the opportunity for attaching metal chelating groups to proteins has increased the opportunities to utilize other radionuclides such as indium  and yttrium . Yttrium  provides several benefits for utilization in radioimmunotherapeutic applications: the 64 hour half-life of yttrium  is long enough to allow antibody accumulation by tumor and, unlike eg, iodine , yttrium  is a pure beta emitter of high energy with no accompanying gamma irradiation in its decay, with a range in tissue of 100 to 1000 cell diameters. Furthermore, the minimal amount of penetrating radiation allows for outpatient administration of yttrium -labeled antibodies. Additionally, interalization of labeled antibody is not required for cell killing, and the local emission of ionizing radiation should be lethal for adjacent tumor cells lacking the target antigen.
One non-therapeutic limitation to yttrium  is based upon the absence of significant gamma radiation making imaging therewith difficult. To avoid this problem, a diagnostic “imaging” radionuclide, such as indium , can be utilized for determining the location and relative size of a tumor prior to the administration of therapeutic does of yttrium -labeled anti-CD20. Indium  is particularly preferred as the diagnostic radionuclide because: between about 1 to about 10 mCi can be safely administered without detectable toxicity; and the imaging data is generally predictive of subsequent yttrium -labeled antibody distribution. Most imaging studies utilize 5 mCi indium -labeled antibody because this dose is both safe and has increased imaging efficiency compared with lower doses, with optimal imaging occurring at three to six days after antibody administration. See, for example, Murray J. L., 26 J. Nuc. Med. 3328 (1985) and Carraguillo, J. A. et al , 26 J. Nuc. Med. 67 (1985).
Effective single treatment dosages (ie, therapeutically effective amount) of yttrium  labeled anti-CD20 antibodies range from between about 5 and about 75 mCi, more preferably between about 10 and about 40 mCi. Effective single treatment non-marrow ablative dosages of iodine  labeled anti-CD20 antibodies range from between about 5 and about 70 mCi, more preferably between about 5 and about 40 mCi. Effective single treatment ablative dosages (ie, may require autologous bone marrow transplantation) of iodine  labeled anti-CD20 antibodies range from between about 30 and about 600 mCi, more preferably between about 50 and less than about 500 mCi. In conjunction with a chimeric anti-CD20 antibody, owing to the longer circulating half life vis-a-vis murine antibodies, an effective single treatment non-marrow ablative dosages of iodine  labeled chimeric anti-CD20 antibodies range from between about 5 and about 40 mCi, more preferably less than about 30 mCi. Imaging criteria for, eg, the indium  label, are typically less than about 5 mCi.
With respect to radiolabeled anti-CD20 antibodies, therapy therewith can also occur using a single therapy treatment or using multiple treatments. Because of the radionuclide component, it is preferred that prior to treatment, peripheral stem cells (“PSC”) or bone marrow (“BM”) be “harvested” for patients experiencing potentially fatal bone marrow toxicity resulting from radiation. BM and/or PSC are harvested using standard techniques, and then purged and frozen for possible reinfusion. Additionally, it is most preferred that prior to treatment a diagnostic dosimetry study using a diagnostic labeled antibody (eg, using indium ) be conducted on the patient, a purpose of which is to ensure that the therapeutically labeled antibody (eg, using yttrium ) will not become unnecessarily “concentrated” in any normal organ or tissue.
Chimeric mouse/human antibodies have been described. See, for example, Morrison, S. L. et al., PNAS 11:6851-6854 (November 1984); European Patent Publication No. 173494; Boulianne. G. L. et al., Nature 312;642 (December 1984); Neubeiger, M. S. et al., Nature 314:268 (March 1985); European Patent Publication No. 125023; Tan et al., J. Immunol. 135:8564 (November 1985); Sun, L. K. et al., Hybridoma 5/1:517 (1986); Sahagan et al., J. Immunol. 137:1066-1074 (1986). See generally, Muron, Nature 312:597 (December 1984); Dickson, Genetic Engineering News 5/3 (March 1985); Marx, Science 229 455 (August 1985); and Morrison Science 229:1202-1207 (September 1985). Robinson et al., in PCT Publication Number WO 88104936, describe a chimeric antibody with human constant region and murine variable region, having specificity to an epitope of CD20; the murine portion of the chimeric antibody of the Robinson references is derived from the 2H7 mouse monoclonal antibody (gamma 2b, kappa). While the reference notes that the described chimeric antibody is a “prime candidate” for the treatment of B cell disorders, this statement can be viewed as no more than a suggestion to those in the art to determine whether or not this suggestion is accurate for this particular antibody, particularly because the reference lacks any data to support an assertion of therapeutic effectiveness, and importantly, data using higher order mammals such as primates or humans.
Methodologies for generating chimeric antibodies are available to those in the art. For example, the light and heavy chains can be expressed separately, using, for example, immunoglobulin light chain and immunoglobulin heavy chains in separate plasmids. These can then be purified and assembled in vitro into complete antibodies; methodologies for accomplishing such assembly have been described. See, for example, Scharff, M., Harvey Lectures 69:125 (1974). In vitro reaction parameters for the formation of IgG antibodies from reduced isolated light and heavy chains have also been described. See, for example, Beychok, S., Cells of Immunoglobulin Synthesis, Academic Press, New York, p. 69, 1979. Co-expression of light and heavy chains in the same cells to achieve intracellular association and linkage of heavy and light chains into complete H2L2 IgG antibodies is also possible. Such co-expression can be accomplished using either the same or different plasmids in the same host cell.
Another approach, and one which is our most preferred approach for developing a chimeric non-human/human anti-CD20 antibody, is based upon utilization of an expression vector which includes, ab initio, DNA encoding heavy and light chain constant regions from a human source. Such a vector allows for inserting DNA encoding non-human variable region such that a variety of non-human anti-CD20 antibodies can be generated, screened and analyzed for various characteristics (eg, type of binding specificity, epitope binding regions, etc.); thereafter, cDNA encoding the light and heavy chain variable regions from a preferred or desired anti-CD20 antibody can be incorporated into the vector. We refer to these types of vectors as Tandem Chimeric Antibody Expression (“TCAE”) vectors. A most preferred TCAE vector which was used to generate immunologically active chimeric anti-CD20 antibodies for therapeutic treatment of lymphomas is TCAE 8. TCAE 8 is a derivative of a vector owned by the assignee of this patent document, referred to as TCAE 5.2 the difference being that in TCAE 5.2, the translation initiation start site of the dominant selectable marker (neomycin phosphostransferase, “NEO”) is a consensus Kozak sequence, while for TCAE 8, this region is a partially impaired consensus Kozak sequence. Details regarding the impact of the initiation start site of the dominant selectable marker of the TCAE vectors (also referred to as “ANEX vector”) vis-a-vis protein expression are disclosed in detail in the co-pending application filed herewith.
TCAE 8 comprises four (4) transcriptional cassettes, and these are in tandem order, ie, a human immunoglobulin light chain absent a variable region; a human immunoglobulin heavy chain absent a variable region; DHFR; and NEO. Each transcriptional cassette contains its own eukaryotic promoter and polyadenylation region (reference is made to FIG. 1 which is a diagrammatic representation of the TCAE 8 vector (SEQ ID. NO:1-2)). Specifically:
1) the CMV promoter/enhancer in front of the immunoglobulin heavy chain is a truncated version of the promoter/enhancer in front of the light chain, from the Nhe I site at −350 to the Sst I site at −16 (see, 41 Cell 521, 1985).
2) a human immunoglobulin light chain constant region was derived via amplification of cDNA by a PCR reaction. In TCAE 8, this was the human immunoglobulin light chain kappa constant region (Kabat numbering, amino acids 108-214, allotype Km 3, (see, Kabat, E. A. “Sequences of proteins of immunological interest,” NIH Publication, Fifth Ed. No. 91-3242, 1991)), and the human immunoglobulin heavy chain gamma 1 constant region (Kabat numbering amino acids 114-478, allotype Gmla, Gmlz). The light chain was isolated from normal human blood (IDEC Pharmaceuticals Corporation, La Jolla, Calif.); RNA therefrom was used to synthesize cDNA which was then amplified using PCR techniques (primers were derived vis-a-vis the consensus from Kabat). The heavy chain was isolated (using PCR techniques) from cDNA prepared from RNA which was in turn derived from cells transfected with a human IgG1 vector (see, 3 Prot. Eng. 531, 1990; vector pNγ162). Two amino acids were changed in the isolated human IgG1 to match the consensus amino acid sequence from Kabat, to wit: amino acid 225 was changed from valine to alanine (GTT to GCA), and amino acid 287 was changed from methionine to lysine (ATG to AAG);
3) The human immunoglobulin light and heavy chain cassettes contain synthetic signal sequences for secretion of the immunoglobulin chains;
4) The human immunoglobulin light and heavy chain cassettes contain specific DNA restriction sites which allow for insertion of light and heavy immunoglobulin variable regions which maintain the transitional reading frame and do not alter the amino acids normally found in immunoglobulin chains;
5) The DHFR cassette contained its own eukaryotic promoter (mouse beta globin major promoter, “BETA”) and polyadenylation region (bovine growth hormone polyadenylation, “BGH”); and
6) The NEO cassette contained its own eukaryotic promoter (BETA) and polyadenylation region (SV40 early polyadenylation, “SV”).
With respect to the TCAE 8 vector and the NEO cassette, the Kozak region was a partially impaired consensus Kozak sequence (SEQ. ID. NO:7) (which included an upstream Cla I site):
ClaI −3 +1
GGGAGCTTGG ATCGAT ccTct ATG Gtt
(In the TCAE 5.2 vector, the change is between the ClaI and ATG regions, to wit: ccAcc.)
The complete sequence listing of TCAE 8 (including the specific components of the four transcriptional cassettes) is set forth in FIG. 2 (SEQ. ID. NO:1).
As will be appreciated by those in the art, the TCAE vectors beneficially allow for substantially reducing the time in generating the immunologically active chimeric anti-CD20 antibodies. Generation and isolation of non-human light and heavy chain variable regions, followed by incorporation thereof within the human light chain constant transcriptional cassette and human heavy chain constant transcriptional cassette, allows for production of immunologically active chimeric anti-CD20 antibodies.
We have derived a most preferred non-human variable region with specificity to the CD20 antigen using a murine source and hybridoma technology. Using polymerase chain reaction (“PCR”) techniques, the murine light and heavy variable regions were cloned directly into the TCAE 8 vector—this is the most preferred route for incorporation of the non-human variable region into the TCAE vector. This preference is principally predicated upon the efficiency of the PCR reaction and the accuracy of insertion. However, other equivalent procedures for accomplishing this task are available. For example, using TCAE 8 (or an equivalent vector), the sequence of the variable region of a non-human anti-CD20 antibody can be obtained, followed by oligonucleotide synthesis of portions of the sequence or, if appropriate, the entire sequence; thereafter, the portions or the entire synthetic sequence can be inserted into the appropriate locations within the vector. Those skilled in the art are credited with the ability to accomplish this task.
Our most preferred immunologically active chimeric anti-CD20 antibodies were derived from utilization of TCAE 8 vector which included murine variable regions derived from monoclonal antibody to CD20; this antibody (to be discussed in detail. infra), is referred to as “2B8.” The complete sequence of the variable regions obtained from 2B8 in TCAE 8 (“anti-CD20 in TCAE 8”) is set forth in FIG. 3 (SEQ. ID. NO:2).
The host cell line utilized for protein expression is most preferably of mammalian origin; those skilled in the art are credited with ability to preferentially determine particular host cell lines which are best suited for the desired gene product to be expressed therein. Exemplary host cell lines include, but are not limited to, DG44 and DUXBII (Chinese Hamster Ovary lines, DHFR minus), HELA (human cervical carcinoma), CVI (monkey kidney line), COS (a derivative of CVI with SV40 T antigen), R1610 (Chinese hamster fibroblast) BALBC/3T3 (mouse fibroblast), HAK (hamster kidney line), SP2/O (mouse myeloma), P3×63-Ag3.653 (mouse myeloma), BFA-lclBPT (bovine endothelial cells), RAJI (human lymphocyte) and 293 (human kidney). Host cell lines are typically available from commercial services, the American Tissue Culture Collection or from published literature.
Preferably the host cell line is either DG44 (“CHO”) or SP2/O. See Urland, G. et al., “Effect of gamma rays and the dihydrofolate reductase locus: deletions and inversions.” Som. Cell & Mol. Gen. 12/6:555-566 (1986), and Shulman, M. et al., “A better cell line for making hybridomas secreting specific antibodies.” Nature 276:269 (1978), respectively. Most preferably, the host cell line is DG44. Transfection of the plasmid into the host cell can be accomplished by any technique available to those in the art. These include, but are not limited to, transfection (including electrophoresis and electroporation), cell fusion with enveloped DNA, microinjection, and infection with intact virus. See, Ridgway, A. A. G. “Mammalian Expression Vectors.” Chapter 24.2, pp. 470-472 Vectors, Rodriguez and Denhardt, Eds. (Butterworths, Boston, Mass. 1988). Most preferably, plasmid introduction into the host is via electroporation.
The following examples are not intended, nor are they to be construed, as limiting the invention. The examples are intended to evidence; dose-imaging using a radiolabeled anti-CD20 antibody (“I2B8”); radiolabeled anti-CD20 antibody (“Y2B8”); and immunologically active, chimeric anti-CD20 antibody (“C2B8”) derived utilizing a specific vector (“TCAE 8”) and variable regions derived from murine anti-CD20 monoclonal antibody (“2B8”).
I. RADIOLABELED ANTI-CD20 ANTIBODY 2B8
A Anti-CD20 Monoclonal Antibody (Murine) Production (“2B8”)
BALB/C mice were repeatedly immunized with the human lymphoblastoid cell line SB (see, Adams, R. A. et al., “Direct implantation and serial transplantation of human acute lymphoblastic leukemia in hamsters, SB-2.” Can Res 28:1121-1125 (1968); this cell line is available from the American Tissue Culture Collection, Rockville, Md., under ATCC accession number ATCC CCL 120), with weekly injections over a period of 3-4 months. Mice evidencing high serum titers of anti-CD20 antibodies, as determined by inhibition of known CD20-specific antibodies (anti-CD20 antibodies utilized were Leu 16, Beckton Dickinson, San Jose, Calif., Cat. No. 7670; and Bl, Coulter Corp., Hialeah, Fla., Cat. No. 6602201) were identified; the spleens of such mice were then removed. Spleen cells were fused with the mouse myeloma SP2/0 in accordance with the protocol described in Einfeld, D. A. et al., (1988) EMBO 7:711 (SP2/0 has ATCC accession no. ATCC CRL 8006).
Assays for CD20 specificity were accomplished by radioimmunoassay. Briefly, purified anti-CD20 Bl was radiolabeled with I125 by the iodobead method as described in Valentine, M. A. et al., (1989) J. Biol. Chem. 264:11282. (I125 Sodium Iodide, ICN, Irvine, Calif., Cat. No. 28665H). Hybridomas were screened by co-incubation of 0.05 ml of media from each of the fusion wells together with 0.05 ml of I125 labeled anti-CD20 Bl (10 ng) in 1% BSA, PBS (pH 7.4), and 0.5 ml of the same buffer containing 100,000 SB cells. After incubation for 1 hr at room temperature, the cells were harvested by transferring to 96 well titer plates (V&P Scientific, San Diego, Calif.), and washed thoroughly. Duplicate wells containing unlabeled anti-CD20 Bl and wells containing no inhibiting antibody were used as positive and negative controls, respectively. Wells containing greater than 50% inhibition were expanded and cloned. The antibody demonstrating the highest inhibition was derived from the cloned cell line designated herein as “2B8.”
B. Preparation of 2B8-MX-DTPA Conjugate
Carbon-14-labeled 1-isothiocyanatobenzyl-3-methyldiethylene triaminepentaacetic acid (“carbon-14 labeled MX-DTPA”) was used as a chelating agent for conjugation of radiolabel to 2B8. Manipulations of MX-DTPA were conducted to maintain metal-free conditions, ie, metal-free reagents were utilized and, when possible, polypropylene plastic containers (flasks, beakers, graduated cylinders, pipette tips) washed with ALCONOX® (a detergent) and rinsed with MILLI-Q® water (purified water), were similarly utilized. MX-DTPA was obtained as a dry solid from Dr. Otto Gansow (National Institute of Health, Bethesda, Md.) and stored desiccated at 4° C. (protected from light), with stock solutions being prepared in MILLI®-Q water at a concentration of 2-5 mM, with storage at −70° C. MX-DTPA was also obtained from Coulter Immunology (Hialeah, Fla.) as the disodium salt in water and stored at −70° C.
ii. Preparation of 2B8
Purified 2B8 was prepared for conjugation with MX-DTPA by transferring the antibody into metal-free 50 mM bicine-NaOff, pH 8.6, containing 150 mM NaCl, using repetitive buffer exchange with CENTRICON 30™ spin filters (30,000D, MWCO; Amicon). Generally, 50-200 μL of protein (10 mg/nl) was added to the filter unit, followed by 2 mL of bicine buffer. The filter was centrifuged at 4° C. in a Sorval SS-34 rotor (6,000 rpm, 45 min.). Retentate volume was approximately 50-100 μL; this process was repeated twice using the same filter. Retentate was transferred to a polypropylene 1.5 mL screw cap tube, assayed for protein, diluted to 10.0 mg/mL and stored at 4° C. until utilized; protein was similarly transferred into 50 mM sodium citrate, pH 5.5, containing 150 mM NaCl and 0.05% sodium azide, using the foregoing protocol.
iii. Conjugation of 2B8 with MX-DTPA
Conjugation of 2B8 with MX-DTPA was performed in polypropylene tubes at ambient temperature. Frozen MX-DTPA stock solutions were thawed immediately prior to use. 50-200 mL of protein at 10 mg/mL were reacted with MX-DTPA at a molar ratio of MX-DTPA-to-2B8 of 4:1. Reactions were initiated by adding the MX-DTPA stock solution and gently mixing; the conjugation was allowed to proceed overnight (14 to 20 hr), at ambient temperature. Unreacted MX-DTPA was removed from the conjugate by dialysis or repetitive ultrafiltration, as described above in Example I.B.ii, into metal-free normal saline (0.9% w/v) containing 0.05% sodium azide. The protein concentration was adjusted to 10 mg/mL and stored at 4° C. in a polypropylene tube until radiolabeled.
iv. Determination of MX-DTPA Incorporation
MX-DTPA incorporation was determined by scintillation counting and comparing the value obtained with the purified conjugate to the specific activity of the carbon--labeled MX-DTPA. For certain studies, in which non-radioactive MX-DTPA (Coulter Immunology) was utilized, MX-DTPA incorporation was assessed by incubating the conjugate with an excess of a radioactive carrier solution of yttrium- of known concentration and specific activity.
A stock solution of yttrium chloride of known concentration was prepared in metal-free 0.05 N HCl to which carrier-free yttrium- (chloride salt) was added. An aliquot of this solution was analyzed by liquid scintillation counting to determine an accurate specific activity for this reagent. A volume of the yttrium chloride reagent equal to 3-times the number of mols of chelate expected to be attached to the antibody, (typically 2 mol/mol antibody), was added to a polypropylene tube, and the pH adjusted to 4.0-4.5 with 2 M sodium acetate. Conjugated antibody was subsequently added and the mixture incubated 15-30 min. at ambient temperature. The reaction was quenched by adding 20 mM EDTA to a final concentration of 1 mM and the pH of the solution adjusted to approximately pH 6 with 2M sodium acetate.
After a 5 min. incubation, the entire volume was purified by high-performance, size-exclusion chromatography (described infra). The eluted protein-containing fractions were combined, the protein concentration determined, and an aliquot assayed for radioactivity. The chelate incorporation was calculated using the specific activity of the yttrium- chloride preparation and the protein concentration.
V. Immunoreactivity of 2B8-MX-DTPA
The immunoreactivity of conjugated 2B8 was assessed using whole-cell ELISA. Mid-log phase SB cells were harvested from culture by centrifugation and washed two times with 1×HBSS. Cells were diluted to 1-2×106 cells/mL in HBSS and aliquoted into 96-well polystyrene microtiter plates at 50,000-100,000 cells/well. The plates were dried under vacuum for 2 h. at 40-45° C. to fix the cells to the plastic; plates were stored dry at −20° C. until utilized. For assay, the plates were warmed to ambient temperature immediately before use, then blocked with 1×PBS, pH 7.2-7.4 containing 1% BSA (2 h). Samples for assay were diluted in 1×PBS/1% BSA, applied to plates and serially diluted (1:2) into the same buffer. After incubating plates for 1 h. at ambient temperature, the plates were washed three times with 1×PBS. Secondary antibody (goat anti-mouse IgG1-specific HRP conjugate 50 μL) was added to wells (1:1500 dilution in 1×PBS/1% BSA) and incubated 1 h. at ambient temperature. Plates were washed four times with 1×PBS followed by the addition of ABTS substrate solution (50 mM sodium citrate, pH 4.5 containing 0.01% ATBS and 0.001% H2O2). Plates were read at 405 nm after 15-30 min. incubation. Antigen-negative HSB cells were included in assays to monitor non-specific binding. Immunoreactivity of the conjugate was calculated by plotting the absorbance values vs. the respective dilution factor and comparing these to values obtained using native antibody (representing 100% immunoreactivity) tested on the same plate; several values on the linear portion of the titration profile were compared and a mean value determined (data not shown).
vi. Preparation of Indium--Labeled 2B8-MX-DTPA (“I2B8”)
Conjugates were radiolabeled with carrier-free indium-. An aliquot of isotope (0.1-2 mCi/mg antibody) in 0.05 M HCL was transferred to a polypropylene tube and approximately one-tenth volume of metal-free 2 M HCl added. After incubation for 5 min., metal-free 2 M sodium acetate was added to adjust the solution to pH 4.0-4.4. Approximately 0.5 mg of 2B8-MX-DTPA was added from a stock solution of 10.0 mg/mL DTPA in normal saline, or 50 mM sodium citrate/150 mM NaCl containing 0.05% sodium azide, and the solution gently mixed immediately. The pH solution was checked with pH paper to verify a value of 4.0-4.5 and the mixture incubated at ambient temperature for 15-30 min. Subsequently, the reaction was quenched by adding 20 mM EDTA to a final concentration of 1 mM and the reaction mixture was adjusted to approximately pH 6.0 using 2 M sodium acetate.
After a 5-10 min. incubation, uncomplexed radioisotope was removed by size-exclusion chromatography. The HPLC unit consisted of Waters Model 6000 or TosoHaas Model TSK-6110 solvent delivery system fitted, respectively, with a Waters U6K or Rheodyne 700 injection valve. Chromatographic separations were performed using a gel permeation column (BioRad SEC-250; 7.5×300 mm or comparable TosoHaas column) and a SEC-250 guard column (7.5×100 mm). The system was equipped with a fraction collector (Pharmacia Frac200) and a UV monitor fitted with a 280 nm filter (Pharmacia model UV-1). Samples were applied and eluted isocratically using 1×PBS, pH 7.4, at 1.0 ml/min flow rate. One-half milliliter fractions were collected in glass tubes and aliquots of these counted in a gamma counter. The lower and upper windows were set to 100 and 500 KeV respectively.
The radioincorporation was calculated by summing the radioactivity associated with the eluted protein peak and dividing this number by the total radioactivity eluted from the column; this value was then expressed as a percentage (data not shown). In some cases, the radioincorporation was determined using instant thin-layer chromatography (“ITLC”). Radiolabeled conjugate was diluted 1:10 or 1:20 in 1×PBS containing or 1×PBS/1 mM DTPA, then 1 μL was spotted 1.5 cm from one end of a 1×5 cm strip of ITLC SG paper. The paper was developed by ascending chromatography using 10% ammonium acetate in methanol:water (1:1;v/v). The strip was dried, cut in half crosswise, and the radioactivity associated with each section determined by gamma counting. The radioactivity associated with the bottom half of the strip (protein-associated radioactivity) was expressed as a percentage of the total radioactivity, determined by summing the values for both top and bottom halves (data not shown).
Specific activities were determined by measuring the radioactivity of an appropriate aliquot of the radiolabeled conjugate. This value was corrected for the counter efficiency (typically 75%) and related to the protein concentration of the conjugate, previously determined by absorbance at 280 nm, and the resulting value expressed as mCi/mg protein.
For some experiments, 2B8-MX-DTPA was radiolabeled with indium  following a protocol similar to the one described above but without purification by HPLC; this was referred to as the “mix-and-shoot” protocol.
vii. Preparation of Yttrium--Labeled 2B8-MX-DTPA (“Y2B8”)
The same protocol described for the preparation of I2B8 was followed for the preparation of the yttrium--labeled 2B8-MX-DTPA (“Y2B8”) conjugate except that 2 ng HCl was not utilized; all preparations of yttrium-labeled conjugates were purified by size-exclusion chromatography as described above.
C. Non-Human Animal Studies.
i. Biodistribution of Radiolabeled 2B8-MX-DTPA
I2B8 was evaluated for tissue biodistribution in six-to-eight week old BALB/c mice. The radiolabeled conjugate was prepared using clinical-grade 2B8-MX-DTPA following the “mix and shoot” protocol described above. The specific activity of the conjugate was 2.3 mCi/mg and the conjugate was formulated in PBS, pH 7.4 containing 50 mg/mL HSA. Mice were injected intravenously with 100 μL of I2B8 (approximately 21 μCi) and groups of three mice were sacrificed by cervical dislocation at 0, 24, 48, and 72 hours. After sacrifice, the tail, heart, lungs, liver, kidney, spleen, muscle, and femur were removed, washed and weighed; a sample of blood was also removed for analysis. Radioactivity associated with each specimen was determined by gamma counting and the percent injected dose per gram tissue subsequently determined. No attempt was made to discount the activity contribution represented by the blood associated with individual organs.
In a separate protocol, aliquots of 2B8-MX-DTPA incubated at 4° C. and 30° C. for 10 weeks were radiolabeled with indium- to a specific activity of 2.1 mCi/mg for both preparations. These conjugates were then used in biodistribution studies in mice as described above.
For dosimetry determinations, 2B8-MX-DTPA was radiolabeled with indium- to a specific activity of 2.3 mCi/mg and approximately 1.1 μCi was injected into each of 20 BALB/c mice. Subsequently, groups of five mice each were sacrificed at 1, 24, 48 and 72 hours and their organs removed and prepared for analysis. In addition, portions of the skin, muscle and bone were removed and processed for analysis; the urine and feces were also collected and analyzed for the 24-72 hour time points.
Using a similar approach, 2B8-MX-DTPA was also radiolabeled with yttrium- and its biological distribution evaluated in BALB/c mice over a 72-hour time period. Following purification by HPLC size exclusion chromatography, four groups of five mice each were injected intravenously with approximately 1 μCi of clinically-formulated conjugate (specific activity:12.2 mCi/mg); groups were subsequently sacrificed at 1, 24, 48 and 72 hours and their organs and tissues analyzed as described above. Radioactivity associated with each tissue specimen was determined by measuring bremstrahlung energy with a gamma scintillation counter. Activity values were subsequently expressed as percent injected dose per gram tissue or percent injected dose per organ. While organs and other tissues were rinsed repeatedly to remove superficial blood, the organs were not perfused. Thus, organ activity values were not discounted for the activity contribution represented by internally associated blood.
ii. Tumor Localization of I2B8
The localization of radiolabeled 2B8-MX-DTPA was determined in athymic mice bearing Ramos B cell tumors. Six-to-eight week old athymic mice were injected subcutaneously (left-rear flank) with 0.1 mL of RPMI-1640 containing 1.2×107 Ramos tumor cells which had been previously adapted for growth in athymic mice. Tumors arose within two weeks and ranged in weight from 0.07 to 1.1 grams. Mice were injected intravenously with 100 μL of indium--labeled 2B8-MX-DTPA (16.7 μCi) and groups of three mice were sacrificed by cervical dislocation at 0, 24, 48, and 72 hours. After sacrifice the tail, heart, lungs, liver, kidney, spleen, muscle, femur, and tumor were removed, washed, weighed; a sample of blood was also removed for analysis. Radioactivity associated with each specimen was determined by gamma counting and the percent injected dose per gram tissue determined.
iii. Biodistribution and Tumor Localization Studies with Radiolabeled 2B8-MX-DTPA
Following the preliminary biodistribution experiment described above (Example I.B.viii.a.), conjugated 2B8 was radiolabeled with indium- to a specific activity of 2.3 mCi/mg and roughly 1.1 μCi was injected into each of twenty BALB/c mice to determine biodistribution of the radiolabeled material. Subsequentially, groups of five mice each were sacrificed at 1, 24, 48 and 72 hours and their organs and a portion of the skin, muscle and bone were removed and processed for analysis. In addition, the urine and feces were collected and analyzed for the 24-72 hour time-points. The level of radioactivity in the blood dropped from 40.3% of the injected dose per gram at 1 hour to 18.9% at 72 hours (data not shown). Values for the heart, kidney, muscle and spleen remained in the range of 0.7-9.8% throughout the experiment. Levels of radioactivity found in the lungs decreased from 14.2% at 1 hour to 7.6% at 72 hours; similarly the respective liver injected-dose per gram values were 10.3% and 9.9%. These data were used in determining radiation absorbed dose estimates I2B8 described below.
The biodistribution of yttrium--labeled conjugate, having a specific activity of 12.2 mCi/mg antibody, was evaluated in BALB/c mice. Radioincorporations of >90% were obtained and the radiolabeled antibody was purified by HPLC. Tissue deposition of radioactivity was evaluated in the major organs, and the skin, muscle, bone, and urine and feces over 72 hours and expressed as percent injected dose/g tissue. Results (not shown) evidenced that while the levels of radioactivity associated with the blood dropped from approximately 39.2% injected dose per gram at 1 hour to roughly 15.4% after 72 hours the levels of radioactivity associated with tail, heart, kidney, muscle and spleen remained fairly constant at 10.2% or less throughout the course of the experiment. Importantly, the radioactivity associated with the bone ranged from 4.4% of the injected dose per gram bone at 1 hour to 3.2% at 72 hours. Taken together, these results suggest that little free yttrium was associated with the conjugate and that little free radiometal was released during the course of the study. These data were used in determining radiation absorbed dose estimates for Y2B8 described below.
For tumor localization studies, 2B8-MX-DTPA was prepared and radiolabeled with 111Indium to a specific activity of 2.7 mCi/mg. One hundred microliters of labeled conjugate (approximately 24 μCi) were subsequently injected into each of 12 athymic mice bearing Ramos B cell tumors. Tumors ranged in weight from 0.1 to 1.0 grams. At time points of 0, 24, 48, and 72 hours following injection, 50 μL of blood was removed by retro-orbital puncture, the mice sacrificed by cervical dislocation, and the tail, heart, lungs, liver, kidney, spleen, muscle, femur, and tumor removed. After processing and weighing the tissues, the radioactivity associated with each tissue specimen was determined using a gamma counter and the values expressed as percent injected dose per gram.
The results (not shown) evidenced that the tumor concentrations of the 111In-2B8-MX-DTPA increased steadily throughout the course of the experiment. Thirteen percent of the injected dose was accumulated in the tumor after 72 hours. The blood levels, by contrast, dropped during the experiment from over 30% at time zero to 13% at 72 hours. All other tissues (except muscle) contained between 1.3 and 6.0% of the injected dose per gram tissue by the end of the experiment; muscle tissue contained approximately 13% of the injected dose per gram.
D. Human Studies
i. 2B8 and 2B8-MX-DTPA: Immunohistology Studies with Human Tissues
The tissue reactivity of murine monoclonal antibody 2B8 was evaluated using a panel of 32 different human tissues fixed with acetone. Antibody 2B8 reacts with the anti-CD20 antigen which had a very restricted pattern of tissue distribution, being observed only in a subset of cells in lymphoid tissues including those of hematopoietic origin.
In the lymph node, immunoreactivity was observed in a population of mature cortical B-lymphocytes as well as proliferating cells in the germinal centers. Positive reactivity was also observed in the peripheral blood, B-cell areas of the tonsils, white pulp of the spleen, and with 40-70% of the medullary lymphocytes found in the thymus. Positive reactivity was also seen in the follicles of the lamina propria (Peyer's Patches) of the large intestines. Finally, aggregates or scattered lymphoid cells in the stroma of various organs, including the bladder, breast, cervix, esophagus, lung, parotid, prostate, small intestine, and stomach, were also positive with antibody 2B8 (data not shown).
All simple epithelial cells, as well as the stratified epithelia and epithelia of different organs, were found to be unreactive. Similarly, no reactivity was seen with neuroectodermal cells, including those in the brain, spinal cord and peripheral nerves. Mesenchymal elements, such as.skeletal and smooth muscle cells, fibroblasts, endothelial cells, and polymorphonuclear inflammatory cells were also found to be negative (data not shown).
The tissue reactivity of the 2B8-MX-DTPA conjugate was evaluated using a panel of sixteen human tissues which had been fixed with acetone. As previously demonstrated with the native antibody (data not shown), the 2B8-M-DTPA conjugate recognized the CD20 antigen which exhibited a highly restricted pattern of distribution, being found only on a subset of cells of lymphoid origin. In the lymph node, immunoreactivity was observed in the B cell population. Strong reactivity was seen in the white pulp of the spleen and in the medullary lymphocytes of the thymus. Immunoreactivity was also observed in scattered lymphocytes in the bladder, heart, large intestines, liver, lung, and uterus, and was attributed to the presence of inflammatory cells present in these tissues. As with the native antibody, no reactivity was observed with neuroectodermal cells or with mesenchymal elements (data not shown).
ii. Clinical Analysis of I2B8 (Imaging) and Y2B8 (Therapy)
a. Phase I/II Clinical Trial Single Dose Therapy Study
A Phase I/II clinical analysis of I2B8 (imaging) followed by treatment with a single therapeutic dose of Y2B8 is currently being conducted. For the single-dose study, the following schema is being followed:
1. Peripheral Stem Cell (PSC) or Bone Marrow (BM) Harvest with Purging;
2. I2B8 Imaging;
3. Y2B8 Therapy (three Dose Levels); and
4. PSC or Autologous BM Transplantation (if necessary based upon absolute neutrophil count below 500/mm3 for three consecutive days or platelets below 20,000/mm3 with no evidence of marrow recovery on bone marrow examination).
The Dose Levels of Y2B8 are as follows:
Three patients are to be treated at each of the dose levels for determination of a Maximum Tolerated Dose (“MTD”).
Imaging (Dosimetry) Studies are conducted as follows: each patient is involved in two in vivo biodistribution studies using I2B8. In the first study, 2 mg of I2B8 (5 mCi), is administered as an intravenous (i.v.) infusion over one hour; one week later 2B8 (ie, unconjugated antibody) is administered by i.v. at a rate not to exceed 250 mg/hr followed immediately by 2 mg of I2B8 (5mCi) administered by i.v. over one hour. In both studies, immediately following the I2B8 infusion, each patient is imaged and imaging is repeated at time t=14-18 hr (if indicated), t=24 hr; t=72 hr; and t=96 hr (if indicated). Whole body average retention times for the indium  label are determined; such determinations are also made for recognizable organs or tumor lesions (“regions of interest”).
The regions of interest are compared to the whole body concentrations of the label; based upon this comparison, an estimate of the localization and concentration of Y2B8 can be determined using standard protocols. If the estimated cumulative dose of Y2B8 is greater than eight (8) times the estimated whole body dose, or if the estimated cumulative dose for the liver exceeds 1500 cGy, no treatment with Y2B8 should occur.
If the imaging studies are acceptible, either 0.0 or 1.0 mg/kg patient body weight of 2B8 is administered by i.v. infusion at a rate not to exceed 250 mg/h. This is followed by administration of Y2B8 (10,20 or 40 mCi) at an i.v. infusion rate of 20 mCi/hr.
b. Phase I/II Clinical Trial: Multiple Dose Therapy Study
A Phase I/II clinical analysis of of Y2B8 is currently being conducted. For the multiple-dose study, the following schema is being followed:
1. PSC or BM Harvest;
2. I2B8 Imaging;
3. Y2B8 Therapy (three Dose Levels) for four doses or a total cumulative dose of 80 mCi; and
4. PSC or Autologous BM Transplantation (based upon decision of medical practitioner).
The Dose Levels of Y2B8 are as follows:
Three patients are to be treated at each of the dose levels for determination of an MTD.
Imaging (Dosimetry) Studies are conducted as follows: A preferred imaging dose for the unlabeled antibody (ie, 2B8) will be determined with the first two patients. The first two patients will receive 100 mg of unlabeled 2B8 in 250 cc of normal saline over 4 hrs followed by 0.5 mCi of I2B8—blood will be sampled for biodistribution data at times t=0, t=10 min., t=120 min., t=24 hr, and t=48 hr. Patients will be scanned with multiple regional gamma camera images at times t=2 hr, t=24 hr and t=48 hr. After scanning at t=48 hr, the patients will receive 250 mg of 2B8 as described, followed by 4.5 mCi of I2B8—blood and scanning will then follow as described. If 100 mg of 2B8 produces superior imaging, then the next two patients will receive 50 mg of 2B8 as described, followed by 0.5 mCi of I2B8 followed 48 hrs later by 100 mg 2B8 and then with 4.5 mCi of I2B8. If 250 mg of 2B8 produces superior imaging, then the next two patients will receive 250 mg of 2B8 as described, followed by 0.5 mCi of I2B8 followed 48 hrs later with 500 mg 2B8 and then with 4.5 mCi of I2B8. Subsequent patients will be treated with the lowest amount of 2B8 that provides optimal imaging. Optimal imaging will be defined by: (1) best effective imaging with the slowest disappearance of antibody; (2) best distribution minimizing compartmentalization in a single organ; and (3) best subjective resolution of the lesion (tumor/background comparison).
For the first four patients, the first therapeutic dose of Y2B8 will begin 14 days after the last dose of I2B8; for subsequent patients, the first therapeutic dose of Y2B8 will begin between two to seven days after the I2B8.
Prior to treatment with Y2B8, for the patients other than the first four, 2B8 will be administered as described, followed by i.v. infusion of Y2B8 over 5-10 min. Blood will be sampled for biodistribution at times t=0, t=10 min., t=120 min., t=24 hr and t=48 hr. Patients will receive repetitive doses of Y2B8 (the same dose administered as with the first dose) approximately every six to eight weeks for a maximum of four doses, or total cumulative dose of 80 mCi. It is most preferred that patients not receive a subsequent dose of Y2B8 until the patients' WBC is greater than/equal to 3,000 and AGC is greater than/equal to 100,000.
Following completion of the three-dose level study, an MTD will be defined. Additional patients will then be enrolled in the study and these will receive the MTD.
A Construction of Chimeric Anti-CD20 Immunoglobulin DNA Expression Vector
RNA was isolated from the 2B8 mouse hybridoma cell (as described in Chomczynki, P. et al., “Single step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.” Anal. Biochem. 162:156-159 (1987)), and cDNA was prepared therefrom. The mouse immunoglobulin light chain variable region DNA was isolated from the cDNA by polymerase chain reaction using a set of DNA primers with homology to mouse light chain signal sequences at the 5′ end and mouse light chain J region at the 3′ end. Primer sequences were as follows:
1. VL Sense (SEQ. ID. NO:8)
5′ ATC AC AGATCT CTC ACC ATC GAT TTT CAG GTG CAG ATT ATC AGC TTC 3′
(The underlined portion is a Bgl II site; the above-lined portion is the start codon.)
2. VL Antisense (SEQ. ID. NO:9)
5′ TGC AGC ATC CGTACG TTT GAT TTC CAG CTT 31′
(The underlined portion is a Bsi WI site.)
See, FIGS. 1 and 2 (SEQ. ID. NO:1) for the corresponding Bgl II and Bsi WI sites in TCAE 8, and FIG. 3 (SEQ. ID. NO:2) for the corresponding sites in anti-CD20 in TCAE 8.
These resulting DNA fragment was cloned directly into the TCAE 8 vector in front of the human kappa light chain constant domain and sequenced. The determined DNA sequence for the murine variable region light chain is set forth in FIG. 4 (SEQ. ID. NOS:3-4); see also FIG. 3, nucleotides 978 through 1362. FIG. 4 further provides the amino acid sequence from this murine variable region, and the CDR and framework regions. The mouse light chain variable region from 2B8 is in the mouse kappa VI family. See, Kabat, supra.
The mouse heavy chain variable region was similarly isolated and cloned in front of the human IgGl constant domains. Primers were as follows:
1. VH Sense (SEQ. ID. NO:10)
5′ GCG GCT CCC ACGCGT GTC CTG TCC CAG 3′
(The underlined portion is an Mlu I site.)
2. VH Antisense (SEQ. ID. NO:11)
5′ GG(G/C) TGT TGT GCTAGC TG(A/C) (A/G)GA GAC (G/A)GT GA 3′
(The underlined portion is an Nhe I site.)
See, FIGS. 1 and 2 for corresponding Mlu I and Nhe I sites in TCAE 8, and FIG. 3 for corresponding sites in anti-CD20 in TCAE 8.
The sequence for this mouse heavy chain is set forth in FIG. 5. (SEQ. ID. NO:5-6); see also FIG. 3, nucleotide 2401 through 2820. FIG. 5 also provides the amino acid sequence from this murine variable region, and the CDR and framework regions. The mouse heavy chain variable region from 2B8 is in the mouse VH2B family. See, Kabat, supra.
B. Creation of Chimeric Anti-CD20 Producing CHO and SP2/0 Transfectomas
Chinese hamster ovary (“CHO”) cells DG44 were grown in SSFM II minus hypoxanthine and thymidine media (Gibco, Grand Island, N.Y., Form No. 91-0456PK); SP2/0 mouse myeloma cells were grown in Dulbecco's Modified Eagles Medium media (“DMEM”) (Irvine Scientific, Santa Ana, Calif., Cat. No. 9024) with 5% fetal bovine serum and 20 ml/L glutamine added. Four million cells were electroporated with either 25 μg CHO or 50 μg SP2/0 plasmid DNA that had been restricted with Not I using a BTX 600 electroporation system (BTX, San Diego, Calif.) in 0.4 ml disposable cuvettes. Conditions were either 210 volts for CHO or 180 volts for SP2/0, 400 microfaradays, 13 ohms. Each electroporation was plated into six 96 well dishes (about 7,000 cells/well). Dishes were fed with media containing G418 (GENETICIN, Gibco, Cat. No. 860-1811) at 400 μg/ml active compound for CHO (media further included 50 μM hypoxanthine and 8 μM thymidine) or 800 μg/ml for SP2/0, two days following electroporation and thereafter 2 or 3 days until colonies arose. Supernatant from colonies was assayed for the presence of chimeric immunoglobulin via an ELISA specific for human antibody. Colonies producing the highest amount of immunoglobulin were expanded and plated into 96 well plates containing media plus methotrexate (25 nM for SP2/0 and 5 nM for CHO) and fed every two or three days. Supernatants were assayed as above and colonies producing the highest amount of immunoglobulin were examined. Chimeric anti-CD20 antibody was purified from supernatant using protein A affinity chromatography.
Purified chimeric anti-CD20 was analyzed by electrophoresis in polyacrylamide gels and estimated to be greater than about 95% pure. Affinity and specificity of the chimeric antibody was determined based upon 2B8. Chimeric anti-CD20 antibody tested in direct and competitive binding assays, when compared to murine anti-CD20 monoclonal antibody 2B8, evidenced comparable affinity and specificity on a number of CD20 positive B cells lines (data not presented). The apparent affinity constant (“Kap”) of the chimeric antibody was determined by direct binding of I125 radiolabeled chimeric anti-CD20 and compared to radiolabeled 2B8 by Scatchard plot; estimated Kap for CHO produced chimeric anti-CD20 was 5.2×10−9 M and for SP2/0 produced antibody, 7.4×10−9M. The estimated Kap for 2B8 was 3.5×10−9 M. Direct competition by radioimmunoassay was utilized to confirm both the specificity and retention of immunoreactivity of the chimeric antibody by comparing its ability to effectively compete with 2B8. Substantially equivalent amounts of chimeric anti-CD20 and 2B8 antibodies were required to produce 50% inhibition of binding to CD20 antigens on B cells (data not presented), ie, there was a minimal loss of inhibiting activity of the anti-CD20 antibodies, presumably due to chimerization.
The results of Example II.B indicate, inter alia, that chimeric anti-CD20 antibodies were generated from CHO and SP2/0 transfectomas using the TCAE 8 vectors, and these chimeric antibodies had substantially the same specificity and binding capability as murine anti-CD20 monoclonal antibody 2B8.
C. Determination of Immunological Activity of Chimeric Anti-CD20 Antibodies
i. Human C1q Analysis
Chimeric anti-CD20 antibodies produced by both CHO and SP2/0 cell lines were evaluated for human C1q binding in a flow cytometry assay using fluorescein labeled C1q (C1q was obtained from Quidel, Mira Mesa, Calif., Prod. No. A400 and FITC label from Sigma, St. Louis Mo., Prod. No. F-7250; FITC. Labeling of C1q was accomplished in accordance with the protocol described in Selected Methods In Cellular Immunology, Michell & Shiigi, Ed. (W.H. Freeman & Co., San Francisco, Calif., 1980, p. 292). Analytical results were derived using a Becton Dickinson FACScan™ flow cytometer (fluorescein measured over a range of 515-545 nm). Equivalent amounts of chimeric anti-CD20 antibody, human IgG1,K myeloma protein (Binding Site, San Diego, Calif., Prod. No. BP078), and 2B8 were incubated with an equivalent number of CD20-positive SB cells, followed by a wash step with FACS buffer (0.2% BSA in PBS, pH 7.4, 0.02% sodium azide) to remove unattached antibody, followed by incubation with FITC labeled C1q. Following a 30-60 min. incubation, cells were again washed. The three conditions, including FITC-labeled C1q as a control, were analyzed on the FACScan™ following manufacturing instructions. Results are presented in FIG. 6.
As the results of FIG. 6 evidence, a significant increase in fluorescence was observed only for the chimeric anti-CD20 antibody condition; ie, only SB cells with adherent chimeric anti-CD20 antibody were C1q positive, while the other conditions produced the same pattern as the control.
ii. Complement Dependent Cell Lyses
Chimeric anti-CD20 antibodies were analyzed for their ability to lyse lymphoma cell lines in the presence of human serum (complement source). CD20 positive SB cells were labeled with 51Cr by admixing 100 μ Ci of 51Cr with 1×106 SB cells for 1 hr at 37° C.; labeled SB cells were then incubated in the presence of equivalent amounts of human complement and equivalent amounts (0-50 μg/ml) of either chimeric anti-CD20 antibodies or 2B8 for 4 hrsat 37° C. (see, Brunner. K. T. et al., “Quantitative assay of the lytic action of immune lymphoid cells on 51Cr-labeled allogeneic target cells in vitro.” Immunology 14:181-189 (1968). Results are presented in FIG. 7.
The results of FIG. 7 indicate, inter alia, that chimeric anti-CD20 antibodies produced significant lysis (49%) under these conditions.
iii. Antibody Dependent Cellular Cytotoxicity Effector Assay
For this study, CD20 positive cells (SB) and CD20 negative cells (T cell leukemia line HSB; see, Adams, Richard, “Formal Discussion,” Can. Res. 27:2479-2482 (1967); ATCC deposit no. ATCC CCL 120.1) were utilized; both were labeled with 51Cr. Analysis was conducted following the protocol described in Brunner, K. T. et al., “Quantitative assay of the lytic action of immune lymphoid cells on 51Cr-labeled allogeneic target cells in vitro; inhibition by isoantibody and drugs.” Immunology 14:181-189 (1968); a substantial chimeric anti-CD20 antibody dependent cell mediated lysis of CD20 positive SB target cells (51Cr-labeled) at the end of a 4 hr, 37° C. incubation, was observed and this effect was observed for both CHO and SP2/0 produced antibody (effector cells were human peripheral lymphocytes; ratio of effector cells:target was 100:1). Efficient lysis of target cells was obtained at 3.9 μg/ml. In contrast, under the same conditions, the murine anti-CD20 monoclonal antibody 2B8 had a statistically insignificant effect, and CD20 negative HSB cells were not lysed. Results are presented in FIG. 8.
The results of Example II indicate, inter alia, that the chimeric anti-CD20 antibodies of Example I were immunologically active.
III. DEPLETION OF B CELLS IN VIVO USING CHIMERIC ANTI-CD20
A Non-Human Primate Study
Three separate non-human primate studies were conducted. For convenience, these are referred to herein as “Chimeric Anti-CD20: CHO & SP2/0;” “Chimeric Anti-CD20: CHO;” and “High Dosage Chimeric Anti-CD20.” Conditions were as follows:
Chimeric Anti-CD20: CHO & SP2/0
Six cynomolgus monkeys ranging in weight from 4.5 to 7 kilograms (White Sands Research Center, Alamogordo, N.Mex.) were divided into three groups of two monkeys each. Both animals of each group received the same dose of immunologically active chimeric anti-CD20 antibody. One animal in each group received purified antibody produced by the CHO transfectoma; the other received antibody produced by the SP2/0 transfectoma. The three groups received antibody dosages corresponding to 0.1 mg/kg, 0.4 mg/kg, and 1.6 mg/kg each day for four (4) consecutive days. The chimeric immunologically active anti-CD20 antibody, which was admixed with sterile saline, was administered by intravenous infusion; blood samples were drawn prior to each infusion. Additional blood samples were drawn beginning 24 hrs after the last injection (T═O) and thereafter on days 1, 3, 7, 14 and 28; blood samples were also taken thereafter at biweekly intervals until completion of the study at day 90.
Approximately 5 ml of whole blood from each animal was centrifuged at 2000 RPM for 5 min. Plasma was removed for assay of soluble chimeric anti-CD20 antibody levels. The pellet (containing peripheral blood leukocytes and red blood cells) was resuspended in fetal calf serum for fluorescent-labeled antibody analysis (see, “Fluorescent Antibody Labeling of Lymphoid Cell Population,” infra.).
Chimeric Anti-CD20: CHO
Six cynomolgus monkeys ranging in weight from 4 to 6 kilograms (White Sands) were divided into three groups of two monkeys each. All animals were injected with immunologically active chimeric anti-CD20 antibodies produced from the CHO transfectoma (in sterile saline). The three groups were separated as follows: subgroup 1 received daily intravenous injections of 0.01 mg/kg of the antibody over a four (4) day period; subgroup 2 received daily intravenous injections of 0.4 mg/kg of the antibody over a four (4) day period; subgroup 3 received a single intravenous injection of 6.4 mg/kg of the antibody. For all three subgroups, a blood sample was obtained prior to initiation of treatment; additionally, blood samples were also drawn at T=0, 1, 3, 7, 14 and 28 days following the last injection, as described above, and these samples were processed for fluorescent labeled antibody analysis (see, “Fluorescent Antibody Labeling,” infra.). In addition to peripheral blood B cell quantitation, lymph node biopsies were taken at days 7, 14 and 28 following the last injection, and a single cell preparation stained for quantitation of lymphocyte populations by flow cytometry.
High Dosage Chimeric Anti-CD20
Two cynomolgus monkeys (White Sands) were infused with 16.8 mg/kg of the immunologically active chimeric anti-CD20 antibodies from the CHO transfectomas (in sterile saline) weekly over a period of four consecutive weeks. At the conclusion of the treatment, both animals were anesthetized for removal of bone marrow; lymph node biopsies were also taken. Both sets of tissue were stained for the presence of B lymphocytes using Leu 16 by flow cytometry following the protocol described in Ling, N. R. et al., “B-cell and plasma cell antigens.” Leucocyte Typing III White Cell Differentiations Antigens, A. J. McMichael, Ed. (Oxford University Press, Oxford Ky. 1987), p. 302.
Fluorescent Antibody Labeling of Lymphoid Cell Population
After removal of plasma, leukocytes were washed twice with Hanks Balanced Salt Solution (“HBSS”) and resuspended in a plasma equivalent volume of fetal bovine serum (heat inactivated at 56° C. for 30 min.). A 0.1 ml volume of the cell preparation was distributed to each of six (6), 15 ml conical centrifuge tubes Fluorescein labeled monoclonal antibodies with specificity for the human lymphocyte surface markers CD2 (AMAC, Westbrook, Me.), CD20 (Becton Dickinson) and human IgM (Binding Site, San Diego, Calif.) were added to 3 of the tubes for identifying T and B lymphocyte populations. All reagents had previously tested positive to the corresponding monkey lymphocyte antigens. Chimeric anti-CD20 antibody bound to monkey B cell surface CD20 was measured in the fourth tube using polyclonal goat anti-human IgG coupled with phycoerythrin (AMAC). This reagent was pre-adsorbed on a monkey Ig-sepharose column to prevent cross-reactivity to monkey Ig, thus allowing specific detection and quantitation of chimeric anti-CD20 antibody bound to cells. A fifth tube included both anti-IgM and anti-human IgG reagents for double stained B cell population. A sixth sample was included with no reagents for determination of autofluorescence. Cells were incubated with fluorescent antibodies for 30 min., washed and fixed with 0.5 ml of fixation buffer (0.15 M NaCl, 1% paraformaldehyde, pH 7.4) and analyzed on a Becton Dickinson FACScan™ instrument. Lymphocyte populations were initially identified by forward versus right angle light scatter in a dot-plot bitmap with unlabeled leucocytes. The total lymphocyte population was then isolated by gating out all other events. Subsequent fluorescence measurements reflected only gated lymphocyte specific events.
Depletion of Peripheral Blood B Lymphocytes
No observable difference could be ascertained between the efficacy of CHO and SP2/0 produced antibodies in depleting B cells in vivo, although a slight increase in B cell recovery beginning after day 7 for monkeys injected with chimeric anti-CD20 antibodies derived from CHO transfectomas at dosage levels 1.6 mg/kg and 6.4 mg/kg was observed and for the monkey injected with SP2/0 producing antibody at the 0.4 mg/kg dose level. FIGS. 9A, B and C provide the results derived from the chimeric anti-CD20:CHO & SP2/0 study, with FIG. 9A directed to the 0.4 mg/kg dose level; FIG. 9B directed to the 1.6 mg/kg dose level; and FIG. 9C directed to the 6.4 mg/kg dose level.
As is evident from FIG. 9, there was a dramatic decrease (>95%) in peripheral B cell levels after the therapeutic treatment across all tested dose ranges, and these levels were maintained up to seven (7) days post infusion; after this period, B cell recovery began, and, the time of recovery initiation was independent of dosage levels.
In the Chimeric Anti-CD20:CHO study, a 10-fold lower antibody dosage concentration (0.01 mg/kg) over a period of four daily injections (0.04 mg/kg total) was utilized. FIG. 10 provides the results of this study. This dosage depleted the peripheral blood B cell population to approximately 50% of normal levels estimated with either the anti-surface IgM or the Leu 16 antibody. The results also indicate that saturation of the CD20 antigen on the B lymphocyte population was not achieved with immunologically active chimeric anti-CD20 antibody at this dose concentration over this period of time for non-human primates; B lymphocytes coated with the antibody were detected in the blood samples during the initial three days following therapeutic treatment. However, by day 7, antibody coated cells were undetectable.
Table I summarizes the results of single and multiple doses of immunologically active chimeric anti-CD20 antibody on the peripheral blood populations; single dose condition was 6.4 mg/kg; multiple dose condition was 0.4 mg/kg over four (4) consecutive days (these results were derived from the monkeys described above).
PERIPHERAL BLOOD POPULATION FROM C2B8 PRIMATE STUDY
Anti-Hu IgG +
% B Cell Depletion
*Double staining population which indicates extent of chimeric anti-CD20 coated B cells.
The data summarized in Table I indicates that depletion of B cells in peripheral blood under conditions of antibody excess occurred rapidly and effectively, regardless of single or multiple dosage levels. Additionally, depletion was observed for at least seven (7) days following the last injection, with partial B cell recovery observed by day 21.
Table II summarizes the effect of immunologically active, chimeric anti-CD20 antibodies on cell populations of lymph nodes using the treatment regimen of Table I (4 daily doses of 0.4 mg/kg; 1 dose of 6.4 mg/kg); comparative values for normal lymph nodes (control monkey, axillary and inguinal) and normal bone marrow (two monkeys) are also provided.
CELL POPULATIONS OF LYMPH NODES
Anti-Hu IgG +
% B Lymphocyte Depletion
Anti-Hu IgG +
The results of Table II evidence effective depletion of B lymphocytes for both treatment regimens. Table II further indicates that for the non-human primates, complete saturation of the B cells in the lymphatic tissue with immunologically active, chimeric anti-CD20 antibody was not achieved; additionally, antibody coated cells were observed seven (7) days after treatment, followed by a marked depletion of lymph node B cells, observed on day 14.
Based upon this data, the single High Dosage Chimeric Anti-CD20 study referenced above was conducted, principally with an eye toward pharmacology/toxicology determination. Ie this study was conducted to evaluate any toxicity associated with the administration of the chimeric antibody, as well as the efficacy of B cell depletion from peripheral blood lymph nodes and bone marrow. Additionally, because the data of Table II indicates that for that study, the majority of lymph node B cells were depleted between 7 and 14 days following treatment, a weekly dosing regimen might evidence more efficacious results. Table III summarizes the results of the High Dosage Chimeric Anti-CD20 study.
CELL POPULATIONS OF LYMPH NODES AND BONE MARROW
Lymphocyte Populations (%)
mIgM + anti-C2B8b
Inguinal Lymph Node
aIndicates population stained with Leu 16.
bIndicates double staining population, positive for surface IgM cells and chimeric antibody coated cells.
cIndicates total population staining for chimeric antibody including double staining surface IgM positive cells and single staining (surface IgM negative) cells.
dDays after injection of final 16.8 mg/kg dose.
Both animals evaluated at 22 days post treatment cessation contained less than 5% B cells, as compared to 40% in control lymph nodes (see, Table II, supra). Similarly, in the bone marrow of animals treated with chimeric anti-CD20 antibody, the levels of CD20 positive cells were less than 3% as compared to 11-15% in the normal animals (see, Table II, supra). In the animals evaluated at 36 days post treatment cessation, one of the animals (H) had approximately 12% B cells in the lymph node and 4.4% B cells in bone marrow, while the other (G) had approximately 5% B cells in the lymph node and 0.8% in the bone marrow—the data is indicative of significant B cell depletion.
The results of Example III,A indicate, inter alia, that low doses of immunologically active, chimeric anti-CD20 leads to long-term peripheral blood B cell depletion in primates. The data also indicates that significant depletion of B cell populations was achieved in peripheral lymph nodes and bone marrow when repetitive high doses of the antibody were administered. Continued follow-up on the test animals has indicated that even with such severe depletion of peripheral B lymphocytes during the first week of treatment, no adverse health effects have been observed. Furthermore, as recovery of B cell population was observed, a conclusion to be drawn is that the pluripotent stem cells of these primates were not adversely affected by the treatment.
B. Clinical Analysis of C2B8
i. Phase I/II Clinical Trial of C2B8: Single Dose Therapy Study
Fifteen patients having histologically documented relapsed B cell lymphoma have been treated with C2B8 in a Phase II Clinical Trial. Each patient received a single dose of C2B8 in a dose-escalating study; there were three patients per dose: 10 mg/m2; 50 mg/m2; 100 mg/m2; 250 mg/m2 and 500 mg/m2. Treatment was by i.v. infusion through an 0.22 micron in-line filter with C2B8 being diluted in a final volume of 250 cc or a maximal concentration of 1 mg/ml of normal saline. Initial rate was 50 cc/hr for the first hour; if no toxicity was seen, dose rate was able to be escalated to a maximum of 200 cc/hr.
Toxicity (as indicated by the clinician) ranged from “none”, to “fever” to “moderate” (two patients) to “severe” (one patient); all patients completed the therapy treatment. Peripheral Blood Lymphocytes were analyzed to determine, inter alia, the impact of C2B8 on T-cells and B-cells. Consistently for all patients, Peripheral Blood B Lymphocytes were depleted after infusion with C2B8 and such depletion was maintained for in excess of two weeks.
One patient (receiving 100 mg/2 of C2B8) evidenced a Partial Response to the C2B8 treatment (reduction of greater than 50% in the sum of the products of the perpendicular diameters of all measurable indicator lesions lasting greater than four weeks, during which no new lesions may appear and no existing lesions may enlarge); at least one other patient (receiving 500 mg/m2) evidenced a Minor Response to the C2B8 treatment (reduction of less than 50% but at least 25% in the sum of the products of the two longest perpendicular diameters of all measurable indicator lesions). For presentational efficiency, results of the PBLs are set forth in FIG. 14; data for the patient evidencing a PR is set forth in FIG. 14A; for the patient evidencing an MR, data is set forth in FIG. 14B. In FIG. 14, the following are applicable:=Lymphocytes; =CD3+ cells (T cells);=CD20+ cells; =CD19+ cells; =Kappa; =lambda; and z,7 =C2B8. As evidenced, the B cell markers CD20 and CD19, Kappa and Lambda, were depleted for a period in excess of two weeks; while there was a slight, initial reduction in T-cell counts, these returned to an approximate base-line level in a relatively rapid time-frame.
ii. Phase I/II Clinical Trial of C2B8: Multiple Dose Therapy Study
Patients having histologically confirmed B cell lymphoma with measurable progressive disease are eligible for this study which is separated into two parts: in Phase I, consisting of a dose escalation to characterize dose limiting toxicities and determination of biologically active tolerated dose level, groups of three patients will receive weekly i.v. infusions of C2B8 for a total of four (4) separate infusions. Cumulative dose at each of the three levels will be as follows: 500 mg/m2 (125 mg/m2/infusion); 1000 mg/m2 (250 mg/m2/infusion); 1500 mg/m2 (375 mg/m2/infusion. A biologically active tolerated dose is defined, and will be determined, as the lowest dose with both tolerable toxicity and adequate activity); in Phase II, additional patients will receive the biologically active tolerated dose with an emphasis on determining the activity of the four doses of C2B8.
A combination therapeutic approach using C2B8 and Y2B8 was investigated in a mouse xenographic model (nu/nu mice, female, approximately 10 weeks old) utilizing a B cell lymphoblastic tumor (Ramos tumor cells). For comparative purposes, additional mice were also treated with C2B8 and Y2B8.
Ramos tumor cells (ATCC, CRL 1596) were maintained in culture using RPMI-1640 supplemented with 10% fetal calf serum and glutamine at 37° C. and 5% CO2. Tumors were initiated in nine female nude mice approximately 7-10 weeks old by subcutaneous injection of 1.7×106 Ramos cells in a volume of 0.10 ml (HBSS) using a icc syringe fitted with 25 g needle. All animals were manipulated in a laminar flow hood and all cages, bedding, food and water were autoclaved. Tumor cells were passaged by excising tumors and passing these through a 40 mesh screen; cells were washed twice with 1×HBSS (50 ml) by centrifugation (1300 RPM), resuspended in IX HBSS to 10×106 cells/ml, and frozen at −70° C. until used.
For the experimental conditions, cells from several frozen lots were thawed, pelleted by centrifugation (1300 RPM) and washed twice with 1X HBSS. Cells were then resuspended to approximately 2.0×106 cells/ml. Approximately 9 to 12 mice were injected with 0.10 ml of the cell suspension (s.c.) using a 1 cc syringe fitted with a 25 g needle; injections were made on the animal's left side, approximately mid-region. Tumors developed in approximately two weeks. Tumors were excised and processed as described above. Study mice were injected as described above with 1.67×106 cells in 0.10 ml HBSS.
Based on preliminary dosing experiments, it was determined that 200 mg of C2B8 and 100 μCi of Y2B8 would be utilized for the study. Ninety female nu/nu mice (approximately 10 weeks old) were injected with the tumor cells. Approximately ten days later, 24 mice were assigned to four study groups (six mice/group) while attempting to maintain a comparable tumor size distribution in each group (average tumor size, expressed as a product of length x width of the tumor, was approximately 80 mm2). The following groups were treated as indicated via tail-vain injections using a 100 μl Hamilton syringe fitted with a 25 g needle:
A Normal Saline
B. Y2B8 (100 μCi)
C. C2B8 (200 μg); and
D. Y2B8 (100 μCi)+C2B8 (200 μg)
Groups tested with C2B8 were given a second C2B8 injection (200 μg/mouse) seven days after the initial injection. Tumor measurements were made every two or three days using a caliper.
Preparation of treatment materials were in accordance with the following protocols:
A Preparation of Y2B8
Yttrium- chloride (6 mCi) was transformed to a polypropylene tube and adjusted to pH 4.1-4.4 using metal free 2M sodium acetate. 2B8-MX-DTPA (0.3 mg in normal saline; see above for preparation of 2B8-MX-DTPA) was added and gently mixed by vortexing. After 15 min. incubation, the reaction was quenched by adding 0.05×volume 20 mM EDTA and 0.05×volume 2M sodium acetate. Radioactivity concentration was determined by diluting 5.0 μl of the reaction mixture in 2.5 ml 1×PBS containing 76 mg/ml HSA and 1 mM DTPA (“formulation buffer”); counting was accomplished by adding 10.0 μl to 20 ml of Ecolume™ scintillation cocktail. The remainder of the reactive mixture was added to 3.0 ml formulation buffer, sterile filtered and stored at 2-8° C. until used. Specific activity (14 mCi/mg at time of injection) was calculated using the radioactivity concentration and the calculated protein concentration based upon the amount of antibody added to the reaction mixture. Protein-associated radioactivity was determined using instant thin-layer chromatography. Radioincorporation was 95%. Y2B8 was diluted in formulation buffer immediately before use and sterile-filtered (final radioactivity concentration was 1.0 mCi/ml).
B. Preparation of C2B8
C2B8 was prepared as described above. C2B8 was provided as a sterile reagent in normal saline at 5.0 mg/ml. Prior to injection, the C2B8 was diluted in normal saline to 2.0 mg/ml and sterile filtered.
Following treatment, tumor size was expressed as a product of length and width, and measurements were taken on the days indicated in FIG. 11 (Y2B8 vs. Saline); FIG. 12 (C2B8 vs. Saline); and FIG. 13 (Y2B8+C2B8 vs. Saline). Standard error was also determined.
As indicated in FIG. 13, the combination of Y2B8 and C2B8 exhibited tumoricidal effects comparable to the effects evidenced by either Y2B8 or C2B8.
Alternative therapeutic strategies recognized in view of the foregoing examples are evident. One such strategy employs the use of a therapeutic dose of C2B8 followed within about one week with a combination of either 2B8 and radioabeled 2B8 (eg, Y2B8); or 2B8, C2B8 and, eg Y2B8; or C2B8 and, eg, Y2B8. An additional strategy is utilization of radiolabeled C2B8 —such a strategy allows for utilization of the benefits of the immunologically active portion of C2B8 plus those benefits associated with a radiolabel. Preferred radiolabels include yttrium-90 given the larger circulating half-life of C2B8 versus the murine antibody 2B8. Because of the ability of C2B8 to deplete B-cells, and the benefits to be derived from the use of a radiolabel, a preferred alternative strategy is to treat the patient with C2B8 (either with a single dose or multiple doses) such that most, if not all, peripheral B cells have been depleted. This would then be followed with the use of radiolabeled 2B8; because of the depletion of peripheral B cells, the radiolabeled 2B8 stands an increased chance of targeting tumor cells. Iodine  labeled 2B8 is preferably utilized, given the types of results reported in the literature with this label (see Kaminski). An alternative preference involves the use of a radiolabeled 2B8 (or C2B8) first in an effort to increase the permeability of a tumor, followed by single or multiple treatments with C2B8; the intent of this strategy is to increase the chances of the C2B8 in getting both outside and inside the tumor mass. A further strategy involved the use of chemotherapeutic agenst in combination with C2B8. These strategies include so-called “staggered” treatments, ie, treatment with chemotherapeutic agent, followed by treatment with C2B8, followed by a repetition of this protocol. Alternatively, initial treatment with a single or multiple doses of C2B8, thereafter followed with chemotherapeutic treatement, is viable. Preferred chemotherapeutic agents include, but are not limited to: cyclophlsphamide; doxorubicin; vincristine; and prednisone, See Armitage, J. O. et al., Cancer 50:1695 (1982), incorporated herein by reference.
The foregoing alternative therapy strategies are not intended to be limiting, but rather are presented as being representative.
Anti-CD20 in TCAE 8 (transformed in E. coli for purposes of deposit) was deposited with the American Type Culture Collection (ATCC) on Nov. 4, 1992, 12301 Parklawn Drive, Rockville, Md., 20852, under the provisions of the Budapest Treaty for the International Recognition of the Deposit of Microorganisms for the Purpose of Patent Procedure (“Budapest Treaty”). The microorganism was tested by the ATCC on Nov. 9, 1992, and determined to be viable on that date. The ATCC has assigned this microorganism for the following ATCC deposit number: ATCC 69119 (anti-CD20 in TCAE 8). Hybridoma 2B8 was deposited with the ATCC on Jun. 22, 1993 under the provisions of the Budapest Treaty. The viability of the culture was determined on Jun. 25, 1993 and the ATCC has assigned this hybridoma the following ATCC deposit number: HB 11388.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US5500362||Mar 5, 1991||Mar 19, 1996||Xoma Corporation||Chimeric antibody with specificity to human B cell surface antigen|
|EP0125023B1||Apr 6, 1984||Jun 5, 1991||Genentech, Inc.||Recombinant immunoglobulin preparations, methods for their preparation, dna sequences, expression vectors and recombinant host cells therefor|
|EP0173494A2||Aug 7, 1985||Mar 5, 1986||The Board Of Trustees Of The Leland Stanford Junior University||Chimeric receptors by DNA splicing and expression|
|EP0274394A2||Jan 7, 1988||Jul 13, 1988||Xoma Corporation||Chimeric antibody with specificity to human B cell surface antigen|
|EP0451216B1||Dec 28, 1989||Jan 24, 1996||Protein Design Labs, Inc.||Humanized immunoglobulins and their production and use|
|EP0682040A1||Dec 28, 1989||Nov 15, 1995||Protein Design Labs, Inc.||Humanized immunoglobulins and their production and use|
|WO1988004936A1||Jan 7, 1988||Jul 14, 1988||Int Genetic Eng||Chimeric antibody with specificity to human b cell surface antigen|
|WO1992007466A1||Oct 18, 1991||May 14, 1992||Squibb Bristol Myers Co||Synergistic therapy with combinations of anti-tumor antibodies and biologically active agents|
|1||Alvin Y. Liu et al; "Production Of A Mouse-Human Chimeric Monoclonal Antibody to CD20 With Potent FC-Dependent Biologic Activity"; vol. 139, No. 10, Nov. 15, 1987.|
|2||*||Anderson et al., The Second Annual IBC Int. Conference on Antibody Engineering, Dec. 16-18, 1991.*|
|3||*||Grossbard et al., Blood, vol. 80: 863-878, 1992.*|
|4||Journal of Cellular Biochemistry, Mitchell Reff et al., "Depletion of B Cells in Vivo By A Chimeric Mouse Human Monoclonal Antibody To CD20", vol. 17, Mar. 29, 1993.|
|5||Netherlands Cancer Institute Amsterdam Annual Report 1993; A. Hekman et al., "Immunotherapy"; pp. 47-48.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7381560||Jul 25, 2001||Jun 3, 2008||Biogen Idec Inc.||Expression and use of anti-CD20 antibodies|
|US7422739||Jul 25, 2001||Sep 9, 2008||Biogen Idec Inc.||Anti-CD20 antibodies|
|US7601335||May 19, 2006||Oct 13, 2009||Genentech, Inc.||Pretreatment of a biological sample from an autoimmune disease subject|
|US7682612||Nov 9, 1999||Mar 23, 2010||Biogen Idec Inc.||Treatment of hematologic malignancies associated with circulating tumor cells using chimeric anti-CD20 antibody|
|US7727525||Apr 27, 2007||Jun 1, 2010||City Of Hope||Engineered anti-CD20 antibody fragments for in vivo targeting and therapeutics|
|US7740847||Jul 18, 2005||Jun 22, 2010||Applied Molecular Evolution, Inc.||Variant Fc regions|
|US7744877||Sep 11, 2002||Jun 29, 2010||Biogen Idec Inc.||Expression and use of anti-CD20 Antibodies|
|US7799900||Sep 21, 2010||Genentech, Inc.||Immunoglobulin variants and uses thereof|
|US7820161||May 4, 2000||Oct 26, 2010||Biogen Idec, Inc.||Treatment of autoimmune diseases|
|US7879984||Jul 31, 2008||Feb 1, 2011||Regeneron Pharmaceuticals, Inc.||Human antibodies to human CD20 and method of using thereof|
|US7914785||Mar 29, 2011||Bergen Teknologieverforing As||B-cell depleting agents, like anti-CD20 antibodies or fragments thereof for the treatment of chronic fatigue syndrome|
|US8097713||Dec 13, 2010||Jan 17, 2012||Regeneron Pharmaceuticals, Inc.||Nucleic acid molecules which encode human anti-CD20 antibodies and methods of use thereof|
|US8206711||Jun 26, 2012||Biogen Idec Inc.||Treatment of chronic lymphocytic leukemia using anti-CD20 antibodies|
|US8280711||Mar 12, 2008||Oct 2, 2012||ESBATech, an Alcon Biomedical Research Unit, LLC.||Sequence based engineering and optimization of single chain antibodies|
|US8329172||Aug 18, 2007||Dec 11, 2012||Biogen Idec||Combination therapies for B-cell lymphomas comprising administration of anti-CD20 antibody|
|US8329181||Dec 13, 2011||Dec 11, 2012||Regeneron Pharmaceuticals, Inc.||Methods for treating B-cell lymphoma by administering an anti-CD20 antibody|
|US8372399||Aug 31, 2006||Feb 12, 2013||Cardiac Pacemakers, Inc.||Bispecific antibodies and agents to enhance stem cell homing|
|US8545843||Sep 20, 2010||Oct 1, 2013||Genentech, Inc.||Treatment of vasculitis|
|US8557244||Jul 28, 2000||Oct 15, 2013||Biogen Idec Inc.||Treatment of aggressive non-Hodgkins lymphoma with anti-CD20 antibody|
|US8562992||Oct 22, 2008||Oct 22, 2013||Genentech, Inc.||Immunoglobulin variants and uses thereof|
|US8636995||Aug 31, 2006||Jan 28, 2014||Cardiac Pacemakers, Inc.||Methods and devices to regulate stem cell homing|
|US8821873||Oct 3, 2013||Sep 2, 2014||Biogen Idec Inc.||Treatment of diffuse large-cell lymphoma with anti-CD20 antibody|
|US8883980||Aug 17, 2007||Nov 11, 2014||Roche Glycart Ag||Antigen binding molecules with increased Fc receptor binding affinity and effector function|
|US20020058029 *||Sep 18, 2001||May 16, 2002||Nabil Hanna||Combination therapy for treatment of autoimmune diseases using B cell depleting/immunoregulatory antibody combination|
|US20020159996 *||Nov 5, 2001||Oct 31, 2002||Kandasamy Hariharan||Use of CD23 antagonists for the treatment of neoplastic disorders|
|US20020197255 *||Jul 25, 2001||Dec 26, 2002||Idec Pharmaceuticals Corporation||Therapeutic application of chimeric and radiolabelled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma|
|US20030021781 *||Jul 17, 2001||Jan 30, 2003||Idec Pharmaceuticals Corporation||Therapeutic application of chimeric and radiolabelled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma|
|US20030082172 *||Mar 14, 2002||May 1, 2003||Idec Pharmaceuticals||Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma|
|US20030103971 *||Sep 12, 2002||Jun 5, 2003||Kandasamy Hariharan||Immunoregulatory antibodies and uses thereof|
|US20030147885 *||Sep 11, 2002||Aug 7, 2003||Idec Pharmaceuticals Corporation||Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma|
|US20030180290 *||Nov 12, 2002||Sep 25, 2003||Idec Pharmaceuticals Corporation||Anti-CD80 antibody having ADCC activity for ADCC mediated killing of B cell lymphoma cells alone or in combination with other therapies|
|US20030206903 *||May 19, 2003||Nov 6, 2003||Idec Pharmaceuticals Corporation||Combination therapies for B-cell lynphomas comprising administration of anti-CD20 antibody|
|US20030211107 *||Sep 12, 2002||Nov 13, 2003||Kandasamy Hariharan||Use of CD23 antagonists for the treatment of neoplastic disorders|
|US20040258616 *||Jan 27, 2004||Dec 23, 2004||Idec Pharmaceuticals Corporation||Compositions and methods for treating cancer using IGSF9 and LIV-1|
|US20050070689 *||Jul 24, 2002||Mar 31, 2005||Genentech, Inc.||Taci and br3 polypeptides and uses thereof|
|US20050095243 *||Jun 4, 2004||May 5, 2005||Genentech, Inc.||Combination therapy for B cell disorders|
|US20050112130 *||Nov 5, 2004||May 26, 2005||Bhat Neelima M.||Enhanced B cell cytotoxicity of CDIM binding antibody|
|US20050123540 *||Sep 29, 2004||Jun 9, 2005||Biogen Idec Inc.||Treatment of B cell malignancies using combination of B cell depleting antibody and immune modulating antibody related applications|
|US20050123546 *||Nov 5, 2004||Jun 9, 2005||Glycart Biotechnology Ag||Antigen binding molecules with increased Fc receptor binding affinity and effector function|
|US20050163775 *||Dec 22, 2004||Jul 28, 2005||Genentech, Inc.||Combination therapy for B cell disorders|
|US20050271658 *||May 3, 2005||Dec 8, 2005||Genentech, Inc.||Preventing autoimmune disease|
|US20060002930 *||Apr 15, 2005||Jan 5, 2006||Genentech, Inc.||Treatment of disorders|
|US20060024295 *||Jun 2, 2005||Feb 2, 2006||Genentech, Inc.||Method for treating lupus|
|US20060029543 *||Jul 8, 2005||Feb 9, 2006||Werner Krause||Treatment of B-cell lymphoma|
|US20060034835 *||Jun 7, 2005||Feb 16, 2006||Genentech, Inc.||Immunoglobulin variants and uses thereof|
|US20060051345 *||Jun 2, 2005||Mar 9, 2006||Genentech, Inc.||Method for treating multiple sclerosis|
|US20060062787 *||Jul 21, 2005||Mar 23, 2006||Genentech, Inc.||Method for treating Sjogren's syndrome|
|US20060073146 *||Feb 28, 2005||Apr 6, 2006||Genentech, Inc.||Uses of agonists and antagonists to modulate activity of TNF-related molecules|
|US20060110387 *||Sep 28, 2005||May 25, 2006||Genentech, Inc.||Method for treating vasculitis|
|US20060171950 *||Mar 30, 2006||Aug 3, 2006||Biogen Idec Inc.||Use of cd23 antagonists for the treatment of neoplastic disorders|
|US20060188495 *||Jan 12, 2006||Aug 24, 2006||Genentech, Inc.||Treatment method|
|US20060233797 *||Apr 13, 2006||Oct 19, 2006||Genentech, Inc.||Treatment of inflammatory bowel disease (IBD)|
|US20060246004 *||Feb 6, 2006||Nov 2, 2006||Genentech, Inc.||Antibody variants and uses thereof|
|US20060263349 *||May 19, 2006||Nov 23, 2006||Genentech, Inc.||Pretreatment of a biological sample from an autoimmune disease subject|
|US20060263355 *||Feb 28, 2006||Nov 23, 2006||Joanne Quan||Treatment of bone disorders|
|US20060286100 *||Aug 11, 2006||Dec 21, 2006||Biogen Idec Inc.||Use of CD23 Antagonists for the Treatment of Neoplastic Disorders|
|US20070009519 *||Jul 21, 2006||Jan 11, 2007||Biogen Idec Inc.||Immunoregulatory Antibodies and Uses Thereof|
|US20070025987 *||Sep 28, 2006||Feb 1, 2007||Genentech, Inc.||Method for Treating Vasculitis|
|US20070071674 *||Jul 18, 2006||Mar 29, 2007||Mclachlan Karen||Polynucleotides encoding novel isoforms of IGSF9|
|US20070212733 *||Nov 21, 2006||Sep 13, 2007||Genentech, Inc.||Methods and compositions related to B cell assays|
|US20070280882 *||Apr 27, 2007||Dec 6, 2007||Wu Anna M||Engineered anti-cd20 antibody fragments for in vivo targeting and therapeutics|
|US20080038261 *||Aug 18, 2007||Feb 14, 2008||Biogen Idec Inc.||Combination therapies for b-cell lymphomas comprising administration of anti-cd20 antibody|
|US20080057027 *||Aug 31, 2006||Mar 6, 2008||Cardiac Pacemakers, Inc||Methods and devices to regulate stem cell homing|
|US20080057053 *||Aug 31, 2006||Mar 6, 2008||Cardiac Pacemakers, Inc||Bispecific antibodies and agents to enhance stem cell homing|
|US20080058922 *||Aug 31, 2006||Mar 6, 2008||Cardiac Pacemakers, Inc.||Methods and devices employing vap-1 inhibitors|
|US20080089893 *||Jul 25, 2001||Apr 17, 2008||Idec Pharmaceuticals Corporation||Therapeutic application of chimeric and radiolabelled antibodies to human b lymphocyte restricted differentiation antigen for treatment of b cell lymphoma|
|US20080095771 *||Oct 30, 2007||Apr 24, 2008||Genentech, Inc.||Treatment Method|
|US20080171036 *||Aug 20, 2007||Jul 17, 2008||Anan Chuntharapai||Taci antibodies and uses thereof|
|US20080213167 *||Aug 17, 2007||Sep 4, 2008||Biogen Idec Inc.||Use of cd23 antagonists for the treatment of neoplastic disorders|
|US20080213168 *||Aug 17, 2007||Sep 4, 2008||Biogen Idec Inc.||Use of cd23 antagonists for the treatment of neoplastic disorders|
|US20080299117 *||May 21, 2008||Dec 4, 2008||Barron Hal V||Treatment Method|
|US20090010921 *||Aug 17, 2007||Jan 8, 2009||Glycart Biotechnology Ag||Antigen binding molecules with increased Fc receptor binding affinity and effector function|
|US20090028848 *||Jun 25, 2008||Jan 29, 2009||Esbatech Ag||Sequence based engineering and optimization of single chain antibodies|
|US20090035322 *||Jul 31, 2008||Feb 5, 2009||Regeneron Pharmaceuticals, Inc.||Human Antibodies to Human CD20 and Method of Using Thereof|
|US20090074760 *||Apr 9, 2008||Mar 19, 2009||Grillo-Lopez Antonio J||Use of chimeric anti-cd20 antibody as in vitro or in vivo purging agent in patients receiving bmt or pbsc transplant|
|US20090074780 *||Jun 25, 2008||Mar 19, 2009||David Urech||Methods of modifying antibodies, and modified antibodies with improved functional properties|
|US20090136516 *||May 7, 2004||May 28, 2009||Tedder Thomas F||Cd-20 specific antibodies and methods of employing same|
|US20090155257 *||Oct 22, 2008||Jun 18, 2009||Genentech, Inc.||Immunoglobulin variants and uses thereof|
|US20090226439 *||Apr 17, 2009||Sep 10, 2009||Genentech, Inc.||Method for treating dementia or alzheimer's disease|
|US20100015055 *||Aug 31, 2009||Jan 21, 2010||Genentech, Inc.||Pretreatment of a biological sample from an autoimmune disease subject|
|US20100080769 *||Apr 1, 2010||Biogen Idec Inc.||Treatment of Chronic Lymphocytic Leukemia using Anti-CD20 Antibodies|
|US20100137150 *||Mar 12, 2008||Jun 3, 2010||Esbatech Ag||Sequence Based Engineering and Optimization of Single Chain Antibodies|
|US20100143352 *||Nov 24, 2009||Jun 10, 2010||Genentech, Inc.||Combination therapy for b cell disorders|
|US20100158903 *||Sep 16, 2009||Jun 24, 2010||Craig Smith||Methods for treating progressive multiple sclerosis|
|US20100233121 *||Feb 26, 2010||Sep 16, 2010||Genentech, Inc.||Method for treating multiple sclerosis|
|US20100303810 *||Dec 2, 2010||Genentech, Inc.||Method for treating lupus|
|US20110008250 *||Sep 20, 2010||Jan 13, 2011||Genentech, Inc.||Treatment of Autoimmune Diseases|
|US20110008336 *||Sep 20, 2010||Jan 13, 2011||Genentech, Inc.||Treatment of Autoimmune Diseases|
|US20110008337 *||Sep 20, 2010||Jan 13, 2011||Genetech, Inc.||Treatment of Autoimmune Diseases|
|US20110008338 *||Sep 20, 2010||Jan 13, 2011||Genentech, Inc.||Treatment of Autoimmune Diseases|
|US20110076273 *||Mar 31, 2011||Genentech, Inc.||Highly Concentrated Pharmaceutical Formulations|
|US20110081681 *||Dec 13, 2010||Apr 7, 2011||Regeneron Pharmaceuticals, Inc.||Human antibodies to human cd20 and method of using thereof|
|US20110142836 *||Jun 16, 2011||Olav Mella||B-cell depleting agents for the treatment of chronic fatigue syndrome|
|US20110165159 *||Jul 7, 2011||Biogen Idec Inc.||Use of chimeric anti-cd20 antibody as in vitro or in vivo purging agent in patients receiving bmt or pbsc transplant|
|EP1918305A1||Jul 31, 2000||May 7, 2008||Biogen Idec Inc.||New clinical parameters for determining hematologic toxicity prior to radioimmunotherapy|
|EP1946775A2||Aug 11, 1999||Jul 23, 2008||Biogen Idec Inc.||Combination therapies for B-cell lymphomas comprising administration of anti-CD20 antibody|
|EP1974747A1||Aug 11, 1999||Oct 1, 2008||Biogen Idec Inc.||Combination therapies for B-cell lymphomas comprising administration of anti-CD20 antibody|
|EP2011520A1||Feb 29, 2000||Jan 7, 2009||Biogen Idec Inc.||Kit for Radiolabeling Proteins with Yttrium-90|
|EP2077281A1||Jan 2, 2008||Jul 8, 2009||Bergen Teknologioverforing AS||Anti-CD20 antibodies or fragments thereof for the treatment of chronic fatigue syndrome|
|EP2272868A2||Jun 4, 2004||Jan 12, 2011||Genentech, Inc.||Combination therapy for B cell disorders|
|WO2001010461A1||Jul 31, 2000||Feb 15, 2001||Idec Pharma Corp||New clinical parameters for determining hematologic toxicity prior to radioimmunotherapy|
|WO2005044998A2||Nov 5, 2004||May 19, 2005||Palingen Inc||Enhanced b cell cytotoxicity of cdim binding antibody|
|WO2010075249A2||Dec 21, 2009||Jul 1, 2010||Genentech, Inc.||A method for treating rheumatoid arthritis with b-cell antagonists|
|WO2011100403A1||Feb 10, 2011||Aug 18, 2011||Immunogen, Inc||Cd20 antibodies and uses thereof|
|U.S. Classification||424/133.1, 530/389.7, 424/153.1, 424/156.1, 424/800, 424/155.1, 424/173.1, 530/388.8, 424/144.1, 424/143.1, 424/801, 530/867, 530/388.73, 424/1.49, 424/174.1, 530/809, 530/387.3, 530/388.85, 530/388.22, 530/391.3|
|International Classification||A61K51/08, A61K51/10, C12N15/09, G01N33/53, C12P21/02, C12N5/10, A61K39/395, A61K47/48, A61K31/375, C07K16/28, A61K51/00, A61K31/704, A61K31/664, A61K31/573, A61K45/00, C12N15/02, A61K38/00, C07K16/46, C12R1/91, A61P35/00, C12N5/02, C12P21/08|
|Cooperative Classification||Y10S530/867, Y10S530/808, Y10S424/80, Y10S530/809, Y10S424/801, C07K2319/00, C07K2317/24, A61K51/1027, A61K47/48561, A61K38/00, C07K2317/56, C07K2317/732, A61K2039/505, A61K51/1093, C12N2799/028, C07K16/2887|
|European Classification||A61K51/10B28, A61K51/10Z, A61K51/08Z, A61K47/48T4B28, C07K16/28U|
|Jun 20, 2006||CC||Certificate of correction|
|Dec 15, 2006||AS||Assignment|
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